Remarkable Stereoelectronic Control in the Lewis Base Assisted [2,3]-Rearrangement of Cyclopropenylmethyl Phosphinites-Reference-Cited by-同舟云学术

Remarkable Stereoelectronic Control in the Lewis Base Assisted [2,3]-Rearrangement of Cyclopropenylmethyl Phosphinites

Published:2007-11-17 Issue:26 Volume:9 Page:5501-5504
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Rubina Marina¹,Woodward Eric W.¹,Rubin Michael¹

Affiliation:

1. Department of Chemistry, University of Kansas and Center for Environmentally Beneficial Catalysis, 1251 Wescoe Hall Drive, Lawrence, Kansas 66045-7582

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol702473s

Reference21 articles.

1. Dirhodium(II) tetrakis(carboxamidates) with chiral ligands. Structure and selectivity in catalytic metal-carbene transformations

2. Effective Uses of Dirhodium(II) Tetrakis[methyl 2-oxopyrrolidine-5(R or S)-carboxylate] for Highly Enantioselective Intermolecular Cyclopropenation Reactions

3. Dirhodium(II) Tetra(N-(dodecylbenzenesulfonyl)prolinate) Catalyzed Enantioselective Cyclopropenation of Alkynes

4. A Reactivity/Affinity Switch for Parallel Kinetic Resolution: α-Amino Acid Quasienantiomers and the Resolution of Cyclopropene Carboxylic Acids

5. A New Chiral Rh(II) Catalyst for Enantioselective [2 + 1]-Cycloaddition. Mechanistic Implications and Applications

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