Pheromone synthesis, CXI. An enzyme-mediated synthesis of both enantiomers of seudenol and 1-methyl-2-cyclohexen-1-ol, the aggregation pheromones ofDendroctonus pseudotsugae-Reference-Cited by-同舟云学术

Pheromone synthesis, CXI. An enzyme-mediated synthesis of both enantiomers of seudenol and 1-methyl-2-cyclohexen-1-ol, the aggregation pheromones ofDendroctonus pseudotsugae

Published:1988-09-14 Issue:9 Volume:1988 Page:903-905
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Mori Kenji,Ogoche Jondiko I. J.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference5 articles.

1. Pheromone synthesis, CX. Synthesis of (4S,5R)-5-hydroxy-4-methyl-3-heptanone (Sitophilure), the aggregation pheromone ofSitophilus oryzae andS. zeamais

2. Synthesis of optically active forms of seudenol, the pheromone of douglas fir beetle

3. 1-Methylcyclohex-2-en-1-ol as an aggregation pheromone ofDendroctonus pseudotsugae

4. Synthesis and bioactivity of optically active forms of 1-methyl-2-cyclohexen-1-ol. An aggregation pheromone of dendroctonus pseudotsugae

5. Enzymes in organic synthesis. 35. Stereoselective pig liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters. Optimization of enantiomeric excess via reaction conditions control

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