Designed Chiral Acyl Radical Equivalents. Preparation and Cyclizations of Disymmetrically Substituted 1,3-Dioxabicyclo[4.4.0]decan-2-yl Radicals-Reference-Cited by-同舟云学术

Designed Chiral Acyl Radical Equivalents. Preparation and Cyclizations of Disymmetrically Substituted 1,3-Dioxabicyclo[4.4.0]decan-2-yl Radicals

Published:1997-01-01 Issue:2 Volume:62 Page:275-286
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Stien D.¹,Samy R.¹,Nouguier R.¹,Crich D.¹,Bertrand M. P.¹

Affiliation:

1. LCMO, Associé au CNRS, Faculté des Sciences Saint-Jérôme, Av. Normandie-Niemen, 13397 Marseille Cedex 20, France, and Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961750n

Reference53 articles.

1. Acyclic stereochemical control in free-radical reactions

2. Hydrogen-Bonding as a Stereocontrolling Element in Free-Radical C-Allylation Reactions: Vicinal, Proximal, and Remote Asymmetric Induction in the Amino Acid Series

3. High .beta.-stereoselectivity in asymmetric radical addition to .alpha.-sulfinylcyclopentenones

4. 1,2-Asymmetric induction in radical-mediated allylation of diethyl (2S,3S)-3-bromo-2-oxysuccinates: efficient stereoselectivity enhancement by complexation with Eu(fod)3

5. Altering the Stereochemistry of Allylation Reactions of Cyclic .alpha.-Sulfinyl Radicals with Diarylureas

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