cyclopentenyl

cyclopentenyl
A radical derived from cyclopentene

Wikipedia foundation.

Игры ⚽ Нужно решить контрольную?

Look at other dictionaries:

  • Quinbolone — Drugbox IUPAC name = (8 R ,9 S ,10 R ,13 S ,14 S ,17 S ) 17 (1 Cyclopentenyloxy) 10,13 dimethyl 6,7,8,9,11,12,14,15,16,17 decahydrocyclopenta [a] phenanthren 3 one width = 200 CAS number=2487 63 0 ATC prefix=A14 ATC suffix=AA06 ATC supplemental=… …   Wikipedia

  • Cyclopal — Systematic (IUPAC) name 5 (1 cyclopent 2 enyl) 5 prop 2 enyl 1,3 diazinane 2,4,6 trione Clinical data Pregnancy cat.  …   Wikipedia

  • Ene reaction — The Ene reaction (also known as the Alder ene reaction) is a chemical reaction between an alkene with an allylic hydrogen (the ene) and a compound containing a multiple bond (the enophile), in order to form a new σ bond with migration of the ene… …   Wikipedia

  • Woodward–Hoffmann rules — The Woodward–Hoffmann rules devised by Robert Burns Woodward and Roald Hoffmann are a set of rules in organic chemistry predicting the stereochemistry of pericyclic reactions based on orbital symmetry. These include electrocyclic reactions,… …   Wikipedia

  • Nazarov cyclization reaction — The Nazarov cyclization reaction (often referred to as simply the Nazarov cyclization) is a chemical reaction used in organic chemistry for the synthesis of cyclopentenones. The reaction is typically divided into classical and modern variants,… …   Wikipedia

  • Desymmetrization — in stereochemistry is the modification of a molecule that results in the loss of one or more symmetry elements. An important application involves the introduction of chirality. Formally, such conversion require the loss of an improper axis of… …   Wikipedia

  • oil — oilless, adj. oillessness, n. oillike, adj. /oyl/, n. 1. any of a large class of substances typically unctuous, viscous, combustible, liquid at ordinary temperatures, and soluble in ether or alcohol but not in water: used for anointing, perfuming …   Universalium

  • Désymétrisation — La désymétrisation en stéréochimie est la modification d une molécule qui se traduit par la perte d un ou plusieurs éléments de symétrie, comme celles qui donnent lieu à l apparition de chiralité (perte d un miroir plan, d un centre d inversion… …   Wikipédia en Français

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”