Intramolecular Cyclobutadiene Cycloaddition/Cyclopropanation/Thermal Rearrangement: An Effective Strategy for the Asymmetric Syntheses of Pleocarpenene and Pleocarpenone-Reference-Cited by-同舟云学术

Intramolecular Cyclobutadiene Cycloaddition/Cyclopropanation/Thermal Rearrangement: An Effective Strategy for the Asymmetric Syntheses of Pleocarpenene and Pleocarpenone

Published:2006-12-22 Issue:3 Volume:129 Page:486-487
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Williams Michael J.¹,Deak Holly L.¹,Snapper Marc L.¹

Affiliation:

1. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0674340

Reference39 articles.

1. Diversity-Oriented Synthesis of Biaryl-Containing Medium Rings Using a One Bead/One Stock Solution Platform

2. Diverse Methods for Medium Ring Synthesis

3. Intramolecular Cycloadditions of Cyclobutadiene with Olefins

4. Intramolecular Cycloadditions between Cyclobutadiene and Alkenes

5. Sequential Intramolecular Cyclobutadiene Cycloaddition, Ring-Opening Metathesis, and Cope Rearrangement: Total Syntheses of (+)- and (−)-Asteriscanolide

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