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  2. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2. It consists of a methylene bridge ( −CH 2 − ) attached to a vinyl group ( −CH=CH 2 ). [ 1 ] [ 2 ] The name is derived from the scientific name for garlic , Allium sativum .

  3. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohol is converted mainly to glycidol, which is a chemical intermediate in the synthesis of glycerol, glycidyl ethers, esters, and amines. Also, a variety of polymerizable esters are prepared from allyl alcohol, e.g. diallyl phthalate. [5] Allyl alcohol has herbicidal activity and can be used as a weed eradicant [9]) and fungicide. [8]

  4. Category:Allyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Allyl_compounds

    Pages in category "Allyl compounds" The following 114 pages are in this category, out of 114 total. This list may not reflect recent changes. 0–9. 2C-AL; 2C-T-16; A.

  5. Krische allylation - Wikipedia

    en.wikipedia.org/wiki/Krische_allylation

    The Krische allylation involves “transfer hydrogenative” carbon-carbon bond formations. [16] In a series of papers published in the early 2000s, Krische and coworkers demonstrated that allenes, dienes, and allyl acetates could be converted to transient allylmetal nucleophiles via hydrogenation, transfer hydrogenation or hydrogen auto-transfer. [17]

  6. Carbonyl allylation - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_allylation

    Carbonyl allylation has been employed in the synthesis of polyketide natural products and other oxygenated molecules with a contiguous array of stereocenters. For example, allylstannanation of a threose-derived aldehyde affords the macrolide antascomicin B, which structurally resembles FK506 and rapamycin, and is a potent binder of FKBP12. [12]

  7. Allyl isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Allyl_isothiocyanate

    Allyl isothiocyanate (AITC) is a naturally occurring unsaturated isothiocyanate. The colorless oil is responsible for the pungent taste of cruciferous vegetables such as mustard , radish , horseradish , and wasabi .

  8. Allyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Allyl_cyanide

    Allyl cyanide is an organic compound with the formula CH 2 CHCH 2 CN. Like other small alkyl nitriles, allyl cyanide is colorless and soluble in organic solvents. Allyl cyanide occurs naturally as an antifeedant and is used as a cross-linking agent in some polymers. [2]

  9. Allyl acetate - Wikipedia

    en.wikipedia.org/wiki/Allyl_acetate

    Allyl acetate is an organic compound with formula C 3 H 5 OC(O)CH 3. This colourless liquid is a precursor to especially allyl alcohol , which is a useful industrial intermediate. It is the acetate ester of allyl alcohol.