A New Strategy for the Enantioselective Synthesis of Carba-Prostacyclin Analogues Based on Organocopper Conjugate Addition to a Bicyclic Azoene and Its Application to the Synthesis of 13,14-Dinor-inter-p-phenylene Carbacyclin-Reference-Cited by-同舟云学术

A New Strategy for the Enantioselective Synthesis of Carba-Prostacyclin Analogues Based on Organocopper Conjugate Addition to a Bicyclic Azoene and Its Application to the Synthesis of 13,14-Dinor-inter-p-phenylene Carbacyclin

Published:2002-03-29 Issue:16 Volume:124 Page:4321-4328
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

van Bergen Marc¹,Gais Hans-Joachim¹

Affiliation:

1. Contribution from the Institut für Organische Chemie der Rheinisch-Westfälischen Technischen Hochschule (RWTH) Aachen, Professor-Pirlet-Strasse 1, D-52056 Aachen, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0125772

Reference92 articles.

1. An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation

2. Prostacyclin-analogs

3. Synthesis of therapeutically useful prostaglandin and prostacyclin analogs

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