Enantioselective Synthesis of the Functionalized Bicyclo[2.2.1]heptane Derivatives, Key Intermediates for the Chiral Synthesis of Santalenes and Santalols-Reference-Cited by-同舟云学术

Enantioselective Synthesis of the Functionalized Bicyclo[2.2.1]heptane Derivatives, Key Intermediates for the Chiral Synthesis of Santalenes and Santalols

Published:1986-07-05 Issue:7 Volume:15 Page:1225-1228
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Arai Yoshitsugu,Yamamoto Masatoshi,Koizumi Toru

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference12 articles.

1. Highly diastereoselective Diels-Alder reaction of optically active ethyl 2-p-tolylsulfinylmethylenepropionate with cyclopentadiene

2. The Synthesis of d,l-β-Santalene and d,l-epi-β-Santalene by Stereospecific Routes

3. endo-Dicyclopentadiene Synthesis of (±)-Sesquifenchene and (±)-epi-β-Santalene

4. Stereoselective Syntheses of (�)-epi-?-Santalene and (�)-epi-?-Santalol

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