Modification of C-Terminal Peptides to Form Peptide Enamides: Synthesis of Chondriamides A and C-Reference-Cited by-同舟云学术

Modification of C-Terminal Peptides to Form Peptide Enamides: Synthesis of Chondriamides A and C

Published:2001-10-31 Issue:24 Volume:66 Page:8215-8221
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wang Xiang¹,Porco John A.¹

Affiliation:

1. Department of Chemistry and Center for Streamlined Synthesis, Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215 porco@chem.bu.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0158027

Reference74 articles.

1. Applications of Enamide Chemistry to the Synthesis of Heterocyclc Compounds

2. Preparation of N-Heterocycles by Radical Cyclisation of Enamides Mediated by Manganese(III) or Copper(I). A Comparison of Cyclisation Methods

3. Tandem radical cyclisation of enamides mediated by tin hydride; pyrrolizidinone or indolizidinone ring formation

4. Generation and Trapping of N-Acyliminium Ions Derived from Isomünchnone Cycloadducts. A Versatile Route to Functionalized Heterocycles

5. Generation of 6-(Trifluoromethyl)-4,5-dihydro-2(3H)-pyridone and the Application to Synthesis of Some Fused Nitrogen Heterocycles Carrying a Trifluoromethyl Group on the Bridgehead Position via Radical Cyclization of Dihydropyridones

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