TandemDiels-Alder Reactivity Controlled by Remote Substituents. Regioselective synthesis of linearly annellated six-membered ring systems from (1RS,5SR,6RS,7SR)-6,7-bis(chloromethyl)-8,9-dimethylidene-2-oxabicyclo[3.2.2]nonan-3-one. Crystal structure of (1RS,5RS,6SR,11RS)-6,7-bis(chloromethyl)-3-oxo-2-oxatricyclo[7.4.0.1,5]tridec-8-en-11-yl methyl ketone-Reference-Cited by-同舟云学术

TandemDiels-Alder Reactivity Controlled by Remote Substituents. Regioselective synthesis of linearly annellated six-membered ring systems from (1RS,5SR,6RS,7SR)-6,7-bis(chloromethyl)-8,9-dimethylidene-2-oxabicyclo[3.2.2]nonan-3-one. Crystal structure of (1RS,5RS,6SR,11RS)-6,7-bis(chloromethyl)-3-oxo-2-oxatricyclo[7.4.0.1,5]tridec-8-en-11-yl methyl ketone

Published:1988-08-10 Issue:5 Volume:71 Page:1249-1267
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Demarchi Bernard,Vogel Pierre,Pinkerton Alan A.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference108 articles.

1. Synthesis of polyfunctional, linearly condensed six-membered ring systems by regioselective tandem Diels-Alder additions. Synthesis and reactivity of 6,7-bis(chloromethyl)-8,9-bis(methylene)-2-oxabicyclo[3.2.1]nonan-3-one

2. 193rd ACS meeting in Denver, April 5-10, 1987, Div. of org. chem.

3. ?The Actinomycetes?, The Ronald Press, New York, 1967;

4. ?Encylopaedia of Antibiotics?, 2nd edn., J. Wiley & Sons, New York, 1979;

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