Transition Metal Catalyzed Cycloadditions: An Intramolecular [4 + 4] Cycloaddition Strategy for the Efficient Synthesis of Dicyclopenta[a,d]cyclooctene 5−8−5 Ring Systems-Reference-Cited by-同舟云学术

Transition Metal Catalyzed Cycloadditions: An Intramolecular [4 + 4] Cycloaddition Strategy for the Efficient Synthesis of Dicyclopenta[a,d]cyclooctene 5−8−5 Ring Systems

Published:1997-07-01 Issue:15 Volume:62 Page:4908-4909
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wender Paul A.¹,Nuss John M.¹,Smith David B.¹,Suárez-Sobrino Angel¹,Vågberg Jan¹,Decosta Debra¹,Bordner Jon¹

Affiliation:

1. Department of Chemistry, Stanford University, Stanford, California 94305, and Pfizer Central Research, Groton, Connecticut 06340

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo970841x

Reference38 articles.

1. Fusicoccin. Part III. The structure of fusicoccin H

2. The Structure of Ophiobolin, a C25 Terpenoid Having a Novel Skeleton

3. The isolation of an acyclic C25-isoprenoid alcohol, geranylnerolidol, and a new ophiobolin

4. Enzymic formation of a tricyclic sesterterpene alcohol from mevalonic acid and all-trans-geranylfarnesyl pyrophosphate

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