Asymmetric Cyclopropanations by Rhodium(II) N-(Arylsulfonyl)prolinate Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Alkenes. Practical Enantioselective Synthesis of the Four Stereoisomers of 2-Phenylcyclopropan-1-amino Acid-Reference-Cited by-同舟云学术

Asymmetric Cyclopropanations by Rhodium(II) N-(Arylsulfonyl)prolinate Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Alkenes. Practical Enantioselective Synthesis of the Four Stereoisomers of 2-Phenylcyclopropan-1-amino Acid

Published:1996-01-01 Issue:29 Volume:118 Page:6897-6907
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Davies Huw M. L.¹,Bruzinski Paul R.¹,Lake Debra H.¹,Kong Norman¹,Fall Michael J.¹

Affiliation:

1. Contribution from the Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260-3000, and Department of Chemistry, Wake Forest University, Box 7486, Winston-Salem, North Carolina 27109

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9604931

Reference105 articles.

1. Asymmetric Syntheses of 2,3-Methanoamino Acids

2. Cyclopropane amino acids

3. The structure of coronatine

4. D-Ala2, ΔzPhe4-methionine enkephalin amide, a dehydropeptide hormone

5. Opiate activity of [DAla2,ΔzPhe4]-methionine-enkephalinamide

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