A SIMPLE STEREOSELECTIVE SYNTHESIS OF (lR,3R,5S)-1,3-DIMETHYL-2,9-DIOXABICYCLO[3,3,1]NONANE USING REGIOSELECTIVE RING-OPENING OF (R)-β-METHYL-β-PROPIOLACTONE-Reference-Cited by-同舟云学术

A SIMPLE STEREOSELECTIVE SYNTHESIS OF (lR,3R,5S)-1,3-DIMETHYL-2,9-DIOXABICYCLO[3,3,1]NONANE USING REGIOSELECTIVE RING-OPENING OF (R)-β-METHYL-β-PROPIOLACTONE

Published:1983-09-05 Issue:9 Volume:12 Page:1391-1392
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Sato Toshio,Itoh Toshiyuki,Hattori Chihiro,Fujisawa Tamotsu

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference13 articles.

1. 1,3-Dimethyl-2,9-dioxabicyclo[3.3.1]nonane; A host-specific substance in Norway spruce under attack byTrypodendron lineatum Oliv.

2. GASCHROMATOGRAPHISCH–MASSENSPEKTROMETRISCHE UNTERSUCHUNGEN DER FLÜCHTIGEN RINDENINHALTSSTOFFE VON PICEA ABIES (L.) Karst

3. Synthese vonendo- undexo-1,3-Dimethyl-2,9-dioxa-bicyclo[3.3.1]nonan

4. A novel synthetic method for optically active terpenes by the ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone

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