Stereospecific Overman Rearrangement of Substituted Cyclic Vinyl Bromides: Access to Fully Substituted α-Amino Ketones-Reference-Cited by-同舟云学术

Stereospecific Overman Rearrangement of Substituted Cyclic Vinyl Bromides: Access to Fully Substituted α-Amino Ketones

Published:2019-10-30 Issue:22 Volume:21 Page:8962-8965
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Velasco-Rubio Álvaro¹,Alexy Eric J.¹,Yoritate Makoto¹,Wright Austin C.¹,Stoltz Brian M.¹^ORCID

Affiliation:

1. Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Funder

Xunta de Galicia

National Institute of General Medical Sciences

National Science Foundation

California Institute of Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b03347

Reference40 articles.

1. Chiral Amine Synthesis

2. Recent Advances in Catalytic, Enantioselective α Aminations and α Oxygenations of Carbonyl Compounds

3. Asymmetric Hydrogenation of Prochiral Amino Ketones to Amino Alcohols for Pharmaceutical Use

4. Quaternary centres bearing nitrogen (α-tertiary amines) as products of molecular rearrangements

5. Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamines and Imines

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