Diastereoselective Synthesis of 2,3,5-Trisubstituted Tetrahydrofurans via Cyclofunctionalization Reactions. Evidence of Stereoelectronic Effects-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of 2,3,5-Trisubstituted Tetrahydrofurans via Cyclofunctionalization Reactions. Evidence of Stereoelectronic Effects

Published:2001-11-20 Issue:26 Volume:66 Page:8992-8996
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guindon Yvan¹,Soucy François¹,Yoakim Christiane¹,Ogilvie William W.¹,Plamondon Louis¹

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/jo010873r

Reference24 articles.

1. Allylic strain in six-membered rings

2. Diastereoselective synthesis of 2,3-disubstituted tetrahydrofuran synthons via the iodoetherification reaction. A transition state model based rationalization of the allylic asymmetric induction

3. Stereoselective silver triflate-mediated iodocyclization of carbamates

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

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

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