Synthesis of Methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate via a Hofmann Rearrangement Utilizing Trichloroisocyanuric Acid as an Oxidant-Reference-Cited by-同舟云学术

Synthesis of Methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate via a Hofmann Rearrangement Utilizing Trichloroisocyanuric Acid as an Oxidant

Published:2010-12-06 Issue:1 Volume:76 Page:277-280
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Crane Zackary D.¹,Nichols Paul J.¹,Sammakia Tarek¹,Stengel Peter J.¹

Affiliation:

1. Department of Process Chemistry, Array Bio Pharma Inc., 3200 Walnut Street, Boulder, Colorado 80301, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101504e

Reference58 articles.

1. Asymmetric syntheses of 1-aminocyclopropane-1-carboxylic acid derivatives.

2. Diastereoselective Synthesis of Cyclopropane Amino Acids Using Diazo Compounds Generated in Situ

3. Structure−Activity Study on a Novel Series of Macrocyclic Inhibitors of the Hepatitis C Virus NS3 Protease Leading to the Discovery of BILN 2061

4. Peptide-Based Inhibitors of the Hepatitis C Virus NS3 Protease: Structure−Activity Relationship at the C-Terminal Position

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