Applications of Aziridinium Ions. Selective Syntheses of α,β-Diamino Esters, α-Sulfanyl-β-amino Esters, β-Lactams, and 1,5-Benzodiazepin-2-one-Reference-Cited by-同舟云学术

Applications of Aziridinium Ions. Selective Syntheses of α,β-Diamino Esters, α-Sulfanyl-β-amino Esters, β-Lactams, and 1,5-Benzodiazepin-2-one

Published:2000-10-26 Issue:23 Volume:2 Page:3555-3557
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chuang Tsung-Hsun¹,Sharpless K. Barry¹

Affiliation:

1. Department of Chemistry and the Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol000221%2B

Reference23 articles.

1. Tricarbonyl η6 arene chromium (0) based antitumor agents

2. Covalent structure of a nitrogen mustard-induced DNA interstrand cross-link: an N7-to-N7 linkage of deoxyguanosine residues at the duplex sequence 5'-d(GNC)

3. Treatment of N,N-Dibenzylamino Alcohols with Sulfonyl Chloride Leads to Rearranged β-Chloro Amines, Precursors to β-Amino Acids, and Not to Tetrahydroisoquinolines

4. Synthesis of new potential aminopeptidase inhibitors by Lewis acid induced rearrangement of 2,3-epoxy amines and regiospecific nucleophilic trapping of aziridinium ion intermediates with α-amino esters

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