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organic chemistry, an allene oxide is an epoxide of an allene. The parent compound 2-methylideneoxirane [wd], also known as allene oxide, is CH2=C(−O−)CH2
Allene_oxide
Chemical compound
of allene oxide synthase to form an allene oxide. The rearrangement of allene oxide to form 12-oxophytodienoic acid is catalyzed by the enzyme allene oxide
Jasmonic_acid
In enzymology, an allene-oxide cyclase (EC 5.3.99.6) is an enzyme that belongs to the family of isomerases, specifically a class of other intramolecular
Allene_oxide_cyclase
Any organic compound containing a C=C=C group
In organic chemistry, allenes are organic compounds in which one carbon atom has double bonds with each of its two adjacent carbon atoms (R2C=C=CR2, where
Allene
Index of chemical compounds with the same molecular formula
"Retrodienic reactions XVI - flash thermolytic generation of reactive functional allenes". Tetrahedron Letters. 25 (32): 3459–3460. doi:10.1016/S0040-4039(01)91046-9
C3H4O
Class of enzymes
thromboxane synthase (CYP5), prostacyclin synthase (CYP8), and CYP74A (allene oxide synthase). The active site of cytochrome P450 contains a heme-iron center
Cytochrome_P450
Mediterranean sea in West Asia
Mimura, Tetsuro; Ozeki, Yoshihiro (Fall 1980). "Expression of mangrove allene oxide cyclase enhances salt tolerance in Escherichia coli, yeast, and tobacco
Persian_Gulf
Chemical compound
have a cis,cis-1,4-pentadiene present. Next, an allene oxide synthase occurs followed by allene oxide cyclase. 12-Oxophytodienoic acid is formed. It is
Jasmolone
Biological response in plants
many thigmomorphogenic traits, as demonstrated by mutants deficient in allene oxide synthase (AOS), a key enzyme in the JA biosynthetic pathway, which exhibit
Thigmomorphogenesis
oxidant. These enzymes do not require any reduction system for catalysis. Allene oxide synthase (CYP74A; EC 4.2.1.92), fatty acid hydroperoxide lyase (CYP74B)
P450-containing_systems
synthase EC 5.3.99.5: thromboxane-A synthase EC 5.3.99.6: allene-oxide cyclase EC 5.3.99.7: styrene-oxide isomerase EC 5.3.99.8: capsanthin/capsorubin synthase
List_of_EC_numbers_(EC_5)
intermediate is postulated to occur in ring opening of cyclopropanones, allene oxides and in the Favorskii rearrangement. The intermediate has been produced
Non-Kekulé_molecule
Class of enzymes which convert a molecule between isomeric forms
one part of the molecule to another. In other words, they catalyze the oxidation of one part of the molecule and the concurrent reduction of another part
Isomerase
Biochemical pathway producing octadecanoids
undergoes cyclization by allene oxide cyclase to form 12-oxo-phytodienoic acid. This undergoes reduction and three rounds of beta oxidation to form jasmonic acid
Octadecanoid_pathway
oxidized products. Oxidation of allenes affords allene dioxides or products of intramolecular participation.(6) The oxidations of heteroaromatic compounds
Oxidation_with_dioxiranes
List of Cytochrome P450 enzymes
CYP74A is involved in the dehydration reaction to produce an insatiable allene oxide from hydroperoxide. JA chemical reactions are critical in the presence
Cytochrome P450 (individual enzymes)
Cytochrome_P450_(individual_enzymes)
Chemical compound
Levulinate with (2-Bromoallyl)Diisopropoxyborane Prepared by Haloboration of Allene". Organic Syntheses. 75: 129. doi:10.15227/orgsyn.075.0129. Matyáš, Robert;
Diisopropyl_ether
Scottish professor and researcher of pharmacology
2015. Brash, Alan R (September 2009). "Mechanistic aspects of CYP74 allene oxide synthases and related cytochrome P450 enzymes". Phytochemistry. 70 (13–14):
Alan_Brash_(pharmacologist)
Organic compounds with a carbon-carbon-oxygen ring
to as oxides. Thus, the epoxide of ethylene (C2H4) is ethylene oxide (C2H4O). Many compounds have trivial names; for instance, ethylene oxide is called
Epoxide
olefins. Isomerization of 2-oxyallyl metal complexes to cyclopropanone and allene oxide forms is rapid and reversible; increasing the covalent character of the
Reductive dehalogenation of halo ketones
Reductive_dehalogenation_of_halo_ketones
"Biosynthesis of 12-oxo-10,15(Z)-phytodienoic acid: identification of an allene oxide cyclase". Biochem. Biophys. Res. Commun. 156 (1): 543–50. Bibcode:1988BBRC
Hydroperoxide_dehydratase
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
formula C5H8. The inventory of pentadienes include: 1,2-pentadiene, or ethyl allene, H2C=C=CH−CH2−CH3. It and 2,3-pentadiene are the least common isomers of
Pentadiene
Jernerén F, Hoffmann I, Oliw EH (March 2010). "Linoleate 9R-dioxygenase and allene oxide synthase activities of Aspergillus terreus". Archives of Biochemistry
Linolenate_9R-lipoxygenase
Chemical group (–CH2–CH=CH2)
Other reactions that tend to occur with allylic compounds are selenoxide oxidations, ene reactions, and the Tsuji–Trost reaction. Benzylic groups are related
Allyl_group
Organic compounds of the form >C=O
atom bonded to the carbonyl group, and are therefore more resistant to oxidation. They are oxidized only by powerful oxidizing agents which have the ability
Ketone
Chemical reaction
Molybdenum hexacarbonyl is a carbon monoxide donor in PK-type reactions between allenes and alkynes with dimethyl sulfoxide in toluene. Titanium, nickel, and zirconium
Pauson–Khand_reaction
Chemical compounds with the structure R–O–O–R'
bond, which connects the two main atoms together. Each oxygen atom has a oxidation state of negative one, as 5 of its valence electrons remain in the outermost
Peroxide
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
with one or more functional end-groups such as a hydroxyl group. The term "oxide" or other terms are used for high molar mass polymer when end-groups no
Ether
Organic compound containing the functional group R–CH=O
various sulfoxides (e.g. the Swern oxidation), and amine oxides convert alkyl halides to aldehydes (e.g., the Ganem oxidation). Sterically-hindered nitroxyls
Aldehyde
Chemical compound
it is not encountered in everyday life. It is classified as a carbene, allene and an oxocarbon. Dicarbon monoxide is a product of the photolysis of carbon
Dicarbon_monoxide
Chemical compound
H. J. (1989). "Near-Infrared-Light-Induced Reaction of Singlet SO with Allene and Dimethylacetylene in a Rare Gas Matrix. Infrared Spectra of Two Novel
Sulfur_monoxide
Enzyme
Many of them have anti-parallel β-barrel topology; they all have 2 allene oxide cyclase (AOC) like domain (PF18678), which has featured 8-stranded anti-parallel
Spirotetronate_cyclase_AbyU
Hydrocarbon compound containing one or more C≡C bonds
or transition metals to allenes. Due to their comparable thermodynamic stabilities, the equilibrium constant of alkyne/allene isomerization is generally
Alkyne
Chemical reaction
the oxyallyl cation and prevent isomerization to cyclopropanones and allene oxides. In most cases, an excess of the diene is employed to prevent isomerization
(4+3)_cycloaddition
Anion with formula OCN and charge –1
fulminates as high-energy materials. Fulminates of acetylene, ethylene, and allene". Journal of Energetic Materials, volume 31, issue 7, pages 70-79. doi:10
Cyanate
Organic compound
amount of oxygen (as air) into the plant to establish and maintain a passive oxide layer on exposed stainless steel surfaces. Highly corrosion resistant materials
Urea
Organic compound with a –C≡N functional group
chloroformonitrile oxide [wd] Cl−C≡N+−O−). Nitrile oxides are quite different from nitriles and do not arise from direct oxidation of the latter. Instead
Nitrile
Chemical reaction
Myers, Andrew G.; Zheng, Bin (1996). "New and Stereospecific Synthesis of Allenes in a Single Step from Propargylic Alcohols". Journal of the American Chemical
Mitsunobu_reaction
Chemical group (–CH3) derived from methane
attack by even the strongest acids. The oxidation of a methyl group occurs widely in nature and industry. The oxidation products derived from methyl are hydroxymethyl
Methyl_group
Any organic compound having a sulfanyl group (–SH)
systems, an oxidizing catalyst is used to destroy the odor. A copper-based oxidation catalyst neutralizes the volatile thiols and transforms them into inert
Thiol
Main-group allene analog
1-Phosphaallenes are allenes in which the first carbon atom is replaced by phosphorus, resulting in the structure: -P=C=C<. The first example of a stable
1-Phosphaallenes
Functional group
dithiirane 1-oxide) has been prepared through rearrangement of a 1,3-dithietane. A related compound, 3-(9-triptycyl)dithiirane-1-oxide, was prepared
Thiosulfinate
Chemical group (–N=C=O)
produced by the decarboxylation of alkyl and aryl isocyanate using phosphine oxides as a catalyst: C6H11NCO → (C6H11N)2C + CO2 Ketenimines can be prepared by
Isocyanate
Organic compound or functional group containing a C=N bond
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Imine
Species of flowering plant
caryophyllene oxide. The seed has yielded 11.8% of oil, including 3.3% gadoleic acid and some fatty acids containing the unusual allene group, 25.1% laballenic
Phlomoides_tuberosa
Alkyne hydrocarbon compound with three carbon atoms
CH3C≡CH. It is a component of MAPD gas—along with its isomer propadiene (allene), which was commonly used in gas welding. Unlike acetylene, propyne can
Propyne
Functional group with the chemical structure R–S–S–R′
ferrodoxins is about −430 mV. Disulfide bonds are usually formed from the oxidation of thiol (−SH) groups, especially in biological contexts. The transformation
Disulfide
Chemical compound
core of carbodiimides (N=C=N) is linear, being related to the structure of allene. The molecule has idealized C2 symmetry. The N=C=N moiety gives characteristic
N,N'-Dicyclohexylcarbodiimide
Organic compound with the structure >C(O–)2
azeotropic distillation and trapping water with desiccants like aluminium oxide and molecular sieves. Steps assumed to be involved: protonation of the carbonyl
Acetal
Cyclic chemical group (–C6H5)
possible. The phenyl group is hydrophobic. Phenyl groups tend to resist oxidation and reduction. Phenyl groups (like all aromatic compounds) have enhanced
Phenyl_group
Hydrocarbon compound (H2C=CH2)
oxidized to produce ethylene oxide, a key raw material in the production of surfactants and detergents by ethoxylation. Ethylene oxide is also hydrolyzed to
Ethylene
Chemical group (–C(=O)C6H5
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Benzoyl_group
Organic compounds of the form >C=N–OH
Category:Oximes – specific chemicals containing this functional group Nitrone – the N-oxide of an imine The name "oxime" is derived from "oximide" (i.e., oxy- + amide)
Oxime
Organic molecule containing a neutral carbon with two unbound valence electrons
group. Insertions are another common type of carbene reaction, a form of oxidative addition. Insertions may or may not occur in single step (see above).
Carbene
Hydrocarbon compound containing one or more C=C bonds
two overlapping double bonds (C=C=C) are called allenes—the simplest such compound is itself called allene—and those with three or more overlapping bonds
Alkene
Hydrocarbon ring molecule containing a C≡C bond
The desired product could be obtained as a mixture with the corresponding allene as the major product. Further work in this area was aimed at developing
Cycloalkyne
Organosulfur compounds containing –S(=O)2–N< functional group
acids are deprotonated by amines. They are often prepared by one-pot oxidation of disulfides or thiols linked to amines. An alternative synthesis of
Sulfonamide
Organosulfur compound of the form >S(=O)2
hydrocarbon substituents. Sulfones are typically prepared by organic oxidation of thioethers, often referred to as sulfides. Sulfoxides are intermediates
Sulfone
Organic compound containing C–PO(OR)2 groups
abandoned experimental drug for stroke Organophosphorus compounds Phosphine oxide – OPR3 Phosphinite – P(OR)R2 Phosphonite – P(OR)2R Phosphite – P(OR)3 Phosphinate
Phosphonate
Chemical group (–CH2–CH3)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Ethyl_group
Organic compound containing an –NO2 group
nitrite onto primary halocarbons or organosulfates (the Meyer synthesis). Oxidation of oximes or primary amines. Reduction of β-nitro alcohols or nitroalkenes
Nitro_compound
Organic compounds of the form R–O–O–R′
biological and artificial antioxidants destroy peroxides. In fireflies, oxidation of luciferins, which is catalyzed by luciferases, yields a peroxy compound
Organic_peroxides
Chemical compound
2-butadiene, which is a cumulated diene with structure H2C=C=CH−CH3. This allene has no industrial significance. In 1863, French chemist E. Caventou isolated
Butadiene
Hydrocarbon compound (C6H6)
the products of biological oxidation. Pure benzene, for example, oxidizes in the body to produce an epoxide, benzene oxide, which is not excreted readily
Benzene
Functional group (C=O)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Carbonyl_group
Chemical group (–CH2–C6H5)
multiple names: authors list (link) Johnston, Jeffrey N. (2001), "Chromium(VI) Oxide–3,5-Dimethylpyrazole", Encyclopedia of Reagents for Organic Synthesis, American
Benzyl_group
Chemical compound (H–N=C=O)
fulminates as high energy materials. Fulminates of acetylene, ethylene, and allene". Journal of Energetic Materials. 37 (1): 70–79. Bibcode:2019JEnM...37.
Isocyanic_acid
Organosulfur compound of the form R–SOH
second enzyme, the lachrymatory factor synthase, giving syn-propanethial-S-oxide, (Z)-CH3CH2CH=S+−O−. 2-Propenesulfenic acid [wd], CH2=CHCH2−S−OH, formed
Sulfenic_acid
Polyatomic ion (NO3, charge –1) found in explosives and fertilisers
In the NO3− anion, the oxidation state of the central nitrogen atom is V (+5). This corresponds to the highest possible oxidation number of nitrogen. Nitrate
Nitrate
Chemical group (–CH2–)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Methylene_group
Group of chemical compounds derived from alkanes containing one or more halogens
triphenylphosphine; the co-products are haloform and triphenylphosphine oxide. In the Mitsunobu reaction, the reagents are any nucleophile, triphenylphosphine
Haloalkane
Chemical group (–OH)
ions. Wikimedia Commons has media related to Hydroxyl group. Hydronium Ion Oxide Hydroxylation "Alcohols". Gold Book. IUPAC. February 24, 2014. doi:10.1351/goldbook
Hydroxy_group
Chemical group (–OC(O)CH3)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Acetoxy_group
Chemical reaction
have been developed. In the presence of unpolarized alkenes, alkynes or allenes, diimide is converted into dinitrogen with reduction (net addition of dihydrogen)
Reductions_with_diimide
Chemical group (–CH=CH2)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Vinyl_group
Class of functional groups with a –N=O group attached
organic chemistry, nitroso refers to a functional group in which the nitric oxide (−N=O) group is attached to an organic moiety. As such, various nitroso
Nitroso
Chemical group (–C3H7) derived from propane
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Propyl_group
Heterocyclic aromatic organic compound
increases reactivity to both oxidation and reduction. Oxidation of pyridine occurs at nitrogen to give pyridine N-oxide. The oxidation can be achieved with peracids:
Pyridine
Class of chemical compounds
CH3−SO2−S−CH3 is a colorless liquid. Thiosulfonate esters are usually produced by oxidation of disulfides or the nucleophilic attack of thiolates on organosulfonyl
Thiosulfonate
Organic compounds with a diazenyl group (–N=N–)
temperature, the azo coupling reactions are typically conducted near 0 °C. The oxidation of hydrazines (R−NH−NH−R′) also gives azo compounds. In the opposite direction
Azo_compound
Chemical compound
in wine, but mass production was only possible after the development by Allene Jeanes of a process using bacteria. Dental plaque is rich in dextrans. Dextran
Dextran
Chemical group, –C(=O)CH3
and acetyl-L-carnitine on carnitine levels, ambulatory activity, and oxidative stress biomarkers in the brain of old rats". Annals of the New York Academy
Acetyl_group
Organic molecule with two different functional groups
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Bifunctionality
Chemical group (R–O)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Alkoxy_group
Organic compounds of the form RC(=O)NR′R″
The nickel catalyst breaks the ordinarily strong amide C-N bond through oxidative addition. Many other amide cross-couplings were subsequently developed
Amide
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Reductone
Chemical compound
attributed the cis-configuration to the double bond in the position 16=17. The allene group is responsible for the marked optical activity of the acid. Lamenallenic
Lamenallenic_acid
Organic compounds with the structure >C=S
the chemistry of thiones. For example, thiobenzophenone decomposes upon oxidation to the 3,3,5,5-tetraphenyl-1,2,4-trithiolane (Ph2C)2S3, which arises via
Thioketone
American chemist (1917–2011)
fulvalene, the discoveries of the Doering-LaFlamme allene synthesis and the Parikh-Doering oxidation, prediction of the existence of bullvalene as a fluxional
William_von_Eggers_Doering
Organic compounds with the tautomeric structures RC(S)OH or RC(O)SH
P2S5, generally give poor yields unless catalyzed with triphenylstibine oxide. 2,6-Pyridinedicarbothioic acid is synthesized by treating the diacid dichloride
Thiocarboxylic_acid
Chemical compound
acrylamide is generated by pyrolysis of proteins rich in asparagine. Oxidation of acrylamide, catalyzed by the enzyme cytochrome P450 2E1 (CYP2E1) gives
Glycidamide
Any chemical compound having two acyl groups bonded to the same oxygen atom
the mixed anhydride of 3-phosphoglyceric acid and phosphoric acid. Acidic oxides are also classified as acid anhydrides. The nomenclature of organic acid
Organic_acid_anhydride
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Amide_(functional_group)
5-diene. Such complexes also arise from ring-opening of divinylcyclobutane. Allene is another source of allyl complexes. Reduction of cobalt(II) chloride with
Transition metal allyl complex
Transition_metal_allyl_complex
Organic compounds with the structure R–S(=O)2–OH
methanesulfonic and methanedisulfonic acids. Sulfonic acids can be prepared by oxidation of thiols: RSH + 3/2 O2 → RSO3H Typical oxidants include potassium permanganate
Sulfonic_acid
Class of chemical compounds
tert-butyl hydroperoxide (TBHP) is employed for the production of propylene oxide. Of specialized interest, chiral epoxides are prepared using hydroperoxides
Hydroperoxide
published in the early 2000s, Krische and coworkers demonstrated that allenes, dienes, and allyl acetates could be converted to transient allylmetal
Krische_allylation
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Amine
Nitrogen-based molecule
been recorded (matrix, cryogenic temperatures). One of these has an amine oxide radical group incorporated, another system has a carbon radical group. In
Nitrene
Chemical reaction which transfers an alkyl group between molecules
Butyl Pentyl Methylene Bridge Methine Alkene Vinyl Allyl 1-Propenyl Crotyl Allene Cumulene Aryl Phenyl Benzyl Alkyne Carbene Only carbon, hydrogen, and oxygen
Transalkylation
ALLENE OXIDE
ALLENE OXIDE
Female
English
Variant spelling of Middle English Alvina, ALVENA means "elf friend."
Female
English
Variant spelling of English Alana, possibly ALLANA means "little rock."Â
Girl/Female
Celtic American
Fair, good-looking. Feminine of Allen or.
Girl/Female
Celtic American Dutch
Fair, good-looking. Feminine of Allen or.
Girl/Female
Italian
Famous bearer: Alcine is mistress of alluring enchantments and sensual pleasures in the Orlando...
Surname or Lastname
English and Scottish
English and Scottish : from a Celtic personal name of great antiquity and obscurity. In England the personal name is now usually spelled Alan, the surname Allen; in Scotland the surname is more often Allan. Various suggestions have been put forward regarding its origin; the most plausible is that it originally meant ‘little rock’. Compare Gaelic ailÃn, diminutive of ail ‘rock’. The present-day frequency of the surname Allen in England and Ireland is partly accounted for by the popularity of the personal name among Breton followers of William the Conqueror, by whom it was imported first to Britain and then to Ireland. St. Alan(us) was a 5th-century bishop of Quimper, who was a cult figure in medieval Brittany. Another St. Al(l)an was a Cornish or Breton saint of the 6th century, to whom a church in Cornwall is dedicated.This name was brought to North America from different parts of the British Isles independently by many bearers in the 17th and 18th centuries. Prominent early bearers include Samuel Allen, who settled in Braintree, MA, about 1629 (died 1648 in Windsor, CT) and whose descendants included Ethan Allen (1737–89), leader of the Green Mountain Boys in VT during the Revolution; and William Allen (died 1725), from Dungannon, Ireland, an early Presbyterian settler in Philadelphia, whose descendants include William Allen (1803–79), governor of OH.
Female
English
Variant spelling of English Aline, ALLEEN means "little Eve."Â
Male
English
English name, probably derived from the vocabulary word alpine, ALPINE means "of the Swiss Alps."
Female
English
Scottish Anglicized form of Gaelic AibhilÃn, AILEEN means "little Eve."Â
Girl/Female
Irish American Gaelic Celtic
Beautiful.
Girl/Female
Irish
Ancient Irish name from ail â€noble.â€
Girl/Female
Celtic
Fair, good-looking. Feminine of Allen or.
Female
English
Variant spelling of English Aline, ALLENE means "little Eve."Â
Male
English
English variant spelling of Celtic Alan, possibly ALLEN means "little rock."Â
Female
English
Variant spelling of English Aline, ALLINE means "little Eve."Â
Male
English
Middle English form of Anglo-Saxon Ealdwine, ALDINE means "old friend."
Female
English
Variant spelling of English Aileen, AILENE means "little Eve."Â
Female
English
English variant spelling of French Adeline, ADILENE means "noble."
Female
English
Variant spelling of English Aileen, ALENE means "little Eve."Â
Surname or Lastname
English
English : old spelling of Allen, already well established as a surname in England in Tudor times.
ALLENE OXIDE
ALLENE OXIDE
Boy/Male
Bengali, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
Lord Rama Krishna
Girl/Female
British, English, French, German
Mother of Peace
Boy/Male
Bengali, Indian
Eyes of a Dear
Girl/Female
Hindu, Indian, Marathi, Telugu
Faultless
Girl/Female
Hindu, Indian
Creating Arts
Boy/Male
Tamil
Fresh butter, Gentle, Soft, Always new
Boy/Male
Tamil
Subhransu | ஸà¯à®ªà¯à®°à®¨à®¸à¯
The first drop of nature water, The Moon, White
Boy/Male
Arabic, Indian, Muslim, Persian, Sindhi
Brave
Male
Hindi/Indian
Variant form of Hindi Surendra, SURINDER means "god-Indra."
Boy/Male
Indian, Sanskrit
Sparkling; Beaming
ALLENE OXIDE
ALLENE OXIDE
ALLENE OXIDE
ALLENE OXIDE
ALLENE OXIDE
imp. & p. p.
of Allege
v. t.
To cite or quote; as, to allege the authority of a judge.
v. t.
To allure; to entice.
a.
Of, from, in, or pertaining to, the belly or the intestines; as, alvine discharges; alvine concretions.
pl.
of Alley
v. t.
To bring forward with positiveness; to declare; to affirm; to assert; as, to allege a fact.
a.
Smooth; as, the lene breathing.
n.
One of a group of metameric hydrocarbons, C5H10, of the ethylene series. The colorless, volatile, mobile liquid commonly called amylene is a mixture of different members of the group.
v. t.
To alien or alienate; to transfer, as title or property; as, to aliene an estate.
a.
Not belonging to the same country, land, or government, or to the citizens or subjects thereof; foreign; as, alien subjects, enemies, property, shores.
a.
Of or pertaining to the Alps, or to any lofty mountain; as, Alpine snows; Alpine plants.
n.
Same as Achene.
v. t.
See Allege.
v. t.
To allege again.
pl.
of Alley
n.
One excluded from certain privileges; one alienated or estranged; as, aliens from God's mercies.
a.
Wholly different in nature; foreign; adverse; inconsistent (with); incongruous; -- followed by from or sometimes by to; as, principles alien from our religion.
a.
Letting alone.
a.
Furnished with alleys; forming an alley.
p. pr. & vb. n.
of Allege