Cyclopropenes in the 1,3-Dipolar Cycloaddition with Carbonyl Ylides: Experimental and Theoretical Evidence for the Enhancement of σ-Withdrawal in 3-Substituted-Cyclopropenes-Reference-Cited by-同舟云学术

Cyclopropenes in the 1,3-Dipolar Cycloaddition with Carbonyl Ylides: Experimental and Theoretical Evidence for the Enhancement of σ-Withdrawal in 3-Substituted-Cyclopropenes

Published:2006-05-01 Issue:11 Volume:71 Page:4066-4077
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Diev Vyacheslav V.¹,Kostikov Rafael R.¹,Gleiter Rolf¹,Molchanov Alexander P.¹

Affiliation:

1. Department of Chemistry, Saint Petersburg State University, 198504 Universitetsky pr. 26, Saint Petersburg, Russian Federation, and Organisch-Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 270, D-69120 Heidelberg, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0600656

Reference63 articles.

1. Domino Reactions in Organic Synthesis

2. Sequential Transformations in Organic Chemistry: A Synthetic Strategy with a Future

3. Cascade Processes of Metallo Carbenoids

4. Enantioselective intermolecular 1,3-dipolar cycloaddition via ester-derived carbonyl ylide formation catalyzed by chiral dirhodium(II) carboxylates

5. Total Synthesis of (−)-Colchicine via a Rh-Triggered Cycloaddition Cascade

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