Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7–9-Membered Lactams-Reference-Cited by-同舟云学术

Peptidomimetic Synthesis by Way of Diastereoselective Iodoacetoxylation and Transannular Amidation of 7–9-Membered Lactams

Published:2017-09-26 Issue:19 Volume:19 Page:5066-5069
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Atmuri N. D. Prasad¹^ORCID,Reilley David J.¹,Lubell William D.¹

Affiliation:

1. Département de Chimie, Université de Montréal, P.O. Box 6128, Station Centre-ville, Montréal, Québec H3C 3J7, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02275

Reference35 articles.

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2. The Practice of Ring Constraint in Peptidomimetics Using Bicyclic and Polycyclic Amino Acids

3. St-Cyr, D. J.; García-Ramos, Y.; Doan, N.D.; Lubell, W. D.Peptidomimetics I; Topics in Heterocyclic Chemistry, Vol.48;Lubell, W. D., Ed.Springer-Berlin Heidelberg;Germany, 2017; pp125–176.

4. Design, synthesis, conformational analysis and application of indolizidin-2-one dipeptide mimics

5. Ballet, S.; Guillemyn, K.; Van der Poorten, O.; Schurgers, B.; Verniest, G.; Tourwé, D.Peptidomimetics I; Topics in Heterocyclic Chemistry, Vol.48;Lubell, W. D., Ed.Springer-Berlin Heidelberg,Germany, 2017; pp177–209.

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