Sulfonyl-Stabilized Allylic Norbornenyl and Norbornyl Carbanions: Structure and Stereoselectivity of Reaction with Electrophiles-Reference-Cited by-同舟云学术

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Sulfonyl-Stabilized Allylic Norbornenyl and Norbornyl Carbanions: Structure and Stereoselectivity of Reaction with Electrophiles

Published:1999-07 Issue:7 Volume:1999 Page:1627-1651
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Gais Hans-Joachim,van Gumpel Markus,Raabe Gerhard,Müller Jürgen,Braun Siegmar,Lindner Hans Jörg,Rohs Susanne,Runsink Jan

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference217 articles.

1. Preparation of an optically active prostaglandin intermediate via asymmetric induction

2. New synthetic reactions. Oxidative decarboxylation of .alpha.-methylthiocarboxylic acids, new approach to acyl anion and ketene synthons

3. Stereochemistry of alkylation of carboxylic acid salt and ester .alpha. anions derived from cyclic systems

4. Chiral perturbation of olefins by deuterium substitution. The optical activity and circular dichroism behavior of (1S)-[2-2H]norbornene and deuterated apobornenes

5. Total Synthesis of (±)-Lysergic Acid by an Intramolecular Imino-Diels-AlderReaction. Preliminary communication

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