STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: AN EFFICIENT SYNTHESIS OF (±)-4-METHYLHEPTAN-3-OL, AN AGGREGATION PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE-Reference-Cited by-同舟云学术

STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: AN EFFICIENT SYNTHESIS OF (±)-4-METHYLHEPTAN-3-OL, AN AGGREGATION PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE

Published:1982-08-05 Issue:8 Volume:11 Page:1297-1298
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Koreeda Masato,Tanaka Yoshio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference9 articles.

1. Erythro-selective addition of crotyltrialkyltins to aldehydes regardless of the geometry of the crotyl unit. Stereoselection independent of the stereochemistry of precursors

2. Chemical attractants for the smaller european elm bark beetleScolytus multistriatus (Coleoptera: Scolytidae)

3. Absolute configuration of (−)-4-methylheptan-3-ol, a pheromone of the smaller european elm bark beetle, as determined by the synthesis of its (3R,4R)-(+)- and (3S,4R)-(+)-isomers

4. Stereospezifische Synthese von (+)-(3R, 4R)-4-Methyl-3-heptanol, das Enantiomere eines Pheromons des kleinen Ulmensplintkäfers (Scolytus multistriatus)

5. Preparation des methyl-4 heptanols-3 erythro et threo optiquement purs.

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