The Enantioselective Synthesis of (+)-Estradiol from 1,3-Dihydrobenzo[c]thiophene-2,2-dioxide by Successive Thermal SO2-Extrusion and Cycloaddition Reactions. Preliminary communication-Reference-Cited by-同舟云学术

The Enantioselective Synthesis of (+)-Estradiol from 1,3-Dihydrobenzo[c]thiophene-2,2-dioxide by Successive Thermal SO2-Extrusion and Cycloaddition Reactions. Preliminary communication

Published:1980-09-17 Issue:6 Volume:63 Page:1703-1705
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Oppolzer Wolfgang,Roberts David Anthony

Publisher

Wiley

Subject

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

Reference9 articles.

1. Synthesis, 1978, 793.

2. 1-Substituted 1,3-Dihydroisothianaphthen-2,2-dioxides: Preparation and Use asortho-Quinodimethane Precursors in Intramolecular Cycloadditions. Preliminary communication

3. A remarkably simple, highly efficient, and stereoselective synthesis of steroids and other polycyclic systems. Total synthesis of estra-1,3,5(10)-trien-17-one via intramolecular capture of o-quinodimethanes generated by cheletropic elimination of sulfur dioxide

4. Condensed Cyclobutane Aromatic Compounds. VI. The Pyrolysis of 1,3-Dihydroisothianaphthene-2,2-dioxide: A New Synthesis of Benzocyclobutene1

5. & J. Chem. Soc., 1952, 150.

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