Cyclofunctionalization and Free-Radical-Based Hydrogen-Transfer Reactions. An Iterative Reaction Sequence Applied to the Synthesis of the C7−C16 Subunit of Zincophorin-Reference-Cited by-同舟云学术

Cyclofunctionalization and Free-Radical-Based Hydrogen-Transfer Reactions. An Iterative Reaction Sequence Applied to the Synthesis of the C7−C16 Subunit of Zincophorin

Published:2001-07-07 Issue:16 Volume:66 Page:5427-5437
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guindon Yvan¹,Murtagh Lorraine¹,Caron Valérie¹,Landry Serge R.¹,Jung Grace¹,Bencheqroun Mohammed¹,Faucher Anne-Marie¹,Guérin Brigitte¹

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

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010310f

Reference30 articles.

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

4. Stereoselective chelation-controlled reduction of .alpha.-iodo-.beta.-alkoxy esters under radical conditions

5. The Use of Lewis Acids in Radical Chemistry. Chelation-Controlled Radical Reductions of Substituted α-Bromo-β-alkoxy Esters and Chelation-Controlled Radical Addition Reactions

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