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Synthesis of optically active dihydrocarveol via a stepwise or one-pot enzymatic reduction of (R)- and (S)-carvone

✍ Scribed by Xi Chen; Xiuzhen Gao; Qiaqing Wu; Dunming Zhu


Book ID
116909657
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
318 KB
Volume
23
Category
Article
ISSN
0957-4166

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A simple enantioselective synthesis of (
✍ Masahiko Uchiyama; Masako Oka; Satohide Harai; Akihiro Ohta πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 88 KB

Both enantiomers of 1,7-dioxaspiro[5.5]undecane, the major pheromone components of the olive fruit fly (Bactrocea oleae), have been synthesized by using a new method based on the intramolecular asymmetric oxyselenenylation of 4-(3,4-dihydro-2H-pyran-6-yl)butan-1-ol.