A Stereocontrolled Synthesis of the Pheromone 4‐Methyl‐3‐heptanol: Novel and Selective CC‐Linking Reactions
- 1 April 1982
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 21 (4), 309-310
- https://doi.org/10.1002/anie.198203091
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Diastereoselective Synthesis of β‐Methyl Homoallyl AlcoholsAngewandte Chemie International Edition in English, 1979
- Diastereoselektive Synthese von β‐Methyl‐homoallylalkoholenAngewandte Chemie, 1979
- 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)-(+)-isomersTetrahedron, 1977
- 2-Alkenyl anions and their surprising endo preference. Facile and extreme stereocontrol over carbon-carbon linking reactions with organometallics of the allyl typeJournal of the American Chemical Society, 1976
- Selektive Synthesen mit Organometallen IV: Gezielte Hydroxylierung von AllylstellungenHelvetica Chimica Acta, 1975
- Stéréochimie de l'addition d'organostanniques allyliques aux aldéhydesJournal of Organometallic Chemistry, 1972