Reductive Bergman-Type Cyclizations of Cross-Conjugated Enediynes to Fulvene and Fulvalene Anions: The Role of the Substituent-Reference-Cited by-同舟云学术

Reductive Bergman-Type Cyclizations of Cross-Conjugated Enediynes to Fulvene and Fulvalene Anions: The Role of the Substituent

Published:2006-03-17 Issue:14 Volume:128 Page:4703-4709
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Treitel Noach¹,Eshdat Lior¹,Sheradsky Tuvia¹,Donovan Patrick M.¹,Tykwinski Rik R.¹,Scott Lawrence T.¹,Hopf Henning¹,Rabinovitz Mordecai¹

Affiliation:

1. Contribution from the Department of Organic Chemistry and The Lise Meitner Minerva Center for Computational Chemistry, Safra Campus, The Hebrew University of Jerusalem, Givat Ram, Jerusalem 91904, Israel, Department of Chemistry, University of Alberta, Edmonton, AB T6G2G2, Canada, Merkert Chemistry Center, Department of Chemistry, Boston College, Chestnut Hill, Massachusetts 02467-3860, and Organic Chemistry, Technical University of Braunschweig, Hagenring 30 D-38106 Braunschweig, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0566477

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4. Thermal generation of .alpha.,3-dehydrotoluene from (Z)-1,2,4-heptatrien-6-yne

5. [4+2]-Type Cycloadditions of Tropone and Heptafulvene Derivatives with a Tautomeric Mixture of Cycloheptatrienylidene and Cycloheptatetraene

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