Аннотация:
(2R,6R)-, (2R,6S)-, (2S,6R)- and (2S,6S)-2,6-dimethyloct-1 -yl formates have been prepared from S-(+)- and R-(–)-enantiomers of 3,7-dimethylocta-1,6-diene via enantioselective hydrolysis of (2R/S,6R)- and (2R/S,6S)-2,6-dimethyloct-1-yl formates with porcine pancreatic lipase as the key step.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
G. D. Gamalevich, E. P. Serebryakov, “A Chemico-Enzymatic Synthesis of All Four Stereoisomers of 1,6-Dimethyloct-1-yl Formate, an Aggregation Pheromone Mimic for the Smaller Flour Beetle”, Mendeleev Commun., 4:2 (1994), 40–41
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5142
https://www.mathnet.ru/rus/mendc/v4/i2/p40
Эта публикация цитируется в следующих 3 статьяx:
Michael Larsson, Ba-Vu Nguyen, Hans-Erik Högberg, Erik Hedenström, “Syntheses of the Sixteen Stereoisomers of 3,7,11-Trimethyl-2-tridecanol, Including the (2S,3S,7S,11R) and (2S,3S,7S,11S) Stereoisomers Identified as Pheromone Precursors in Females of the Pine SawflyMicrodiprion pallipes(Hymenoptera: Diprionidae)”, Eur. J. Org. Chem., 2001:2 (2001), 353
G. D. Gamalevich, B. N. Morozov, E. P. Serebryakov, “Terpenes in organic synthesis”, Russ Chem Bull, 45:1 (1996), 196
G. D. GAMALEVICH, E. P. SEREBRYAKOV, “ChemInform Abstract: A Chemico‐Enzymatic Synthesis of All Four Stereoisomers of 2,6‐ Dimethyloct‐1‐yl Formate, an Aggregation Pheromone Mimic for the Smaller Flour Beetle.”, ChemInform, 25:41 (1994)
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