Intramolecular Aminyl and Iminyl Radical Additions to α,β-Unsaturated Esters. Diastereoselective Tandem Cyclofunctionalization and Hydrogen Transfer Reactions-Reference-Cited by-同舟云学术

Intramolecular Aminyl and Iminyl Radical Additions to α,β-Unsaturated Esters. Diastereoselective Tandem Cyclofunctionalization and Hydrogen Transfer Reactions

Published:2001-07-01 Issue:15 Volume:3 Page:2293-2296
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Guindon Yvan¹,Guérin Brigitte¹,Landry Serge R.¹

Affiliation:

1. Institut de recherches cliniques de Montréal (IRCM), Bio-organic Chemistry Laboratory, 110, avenue des Pins Ouest, Montréal, Québec, Canada H2W 1R7, and Department of Chemistry and Department of Pharmacology, Université de Montréal, C.P. 6128, succursale Centre-Ville, Montréal, Québec, Canada H3C 3J7

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0160809

Reference18 articles.

1. Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals. Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction: Synthesis of the C17-C22 Subunit of Ionomycin

2. Role of .sigma.-Donation in the Stereocontrol of Hydrogen-Transfer Reactions Involving Acyclic Radicals

3. The Exocyclic Effect: Protecting Group Strategy to Enhance Stereoselectivity in Hydrogen Transfer Reactions of Acyclic Free Radicals

4. Intramolecular oxygen radical additions to α,β-unsaturated esters. Diastereoselective tandem cyclofunctionalization and hydrogen transfer reactions

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