Chemijos terminų aiškinamasis žodynas – 2-asis patais. ir papild. leid. – Vilnius: Mokslo ir enciklopedijų leidybos institutas. Kazys Daukšas, Jurgis Barkauskas, Vitas Daukšas. 2003.
Enantioselective synthesis — Enantioselective synthesis: Sharpless epoxidation Enantioselective synthesis, also called chiral synthesis, asymmetric synthesis or stereoselective synthesis, is organic synthesis that introduces one or more new and desired elements of… … Wikipedia
enantioselective — adjective (of a catalyst) that catalyzes the reaction of only one of a pair of enantiomers [ … Wiktionary
enantioselective — en·an·tio·se·lec·tive in .ant ē ə sə lek tiv adj relating to or being a chemical reaction in which one enantiomer of a chiral product is preferentially produced en·an·tio·se·lec·tive·ly adv … Medical dictionary
Simmons-Smith reaction — The Simmons Smith reaction is an organic reaction in which a carbenoid reacts with an alkene (or alkyne) to form a cyclopropane. [cite journal | author = Howard Ensign Simmons, Jr.; Smith, R.D. | title = 4 Substituted 2,3,5 pyrrolidinetriones |… … Wikipedia
Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by … Wikipedia
Johnson–Corey–Chaykovsky reaction — The Johnson–Corey–Chaykovsky reaction (sometimes referred to as the Corey–Chaykovsky reaction or CCR) is a chemical reaction used in organic chemistry for the synthesis of epoxides, aziridines, and cyclopropanes. It was discovered in 1961 by A.… … Wikipedia
Michael reaction — The Michael reaction or Michael addition is the nucleophilic addition of a carbanion or another nucleophile[1][2][3] to an alpha, beta unsaturated carbonyl compound. It belongs to the larger class of conjugate additions. This is one of the most… … 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
Nitroaldol reaction — The Henry Reaction (also referred to as the nitro aldol reaction) is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by L. Henry, it is the combination of a nitroalkane and an aldehyde or ketone in the… … Wikipedia
Baylis–Hillman reaction — The Baylis–Hillman reaction is an organic reaction of an aldehyde and an α,β unsaturated electron withdrawing group catalyzed by DABCO (1,4 diazabicyclo[2.2.2]octane) to give an allylic alcohol.[1][2] This reaction is also known as the… … Wikipedia
