Palladium(0)-Catalyzed Regioselective Synthesis of α-Dehydro-β-amino Esters from Amines and Allyl Acetates: Synthesis of a α-Dehydro-β-amino Acid Derived Cyclic Peptide as a Constrained β-Turn Mimic-Reference-Cited by-同舟云学术

Palladium(0)-Catalyzed Regioselective Synthesis of α-Dehydro-β-amino Esters from Amines and Allyl Acetates: Synthesis of a α-Dehydro-β-amino Acid Derived Cyclic Peptide as a Constrained β-Turn Mimic

Published:2002-10-03 Issue:22 Volume:67 Page:7852-7857
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rajesh S.¹,Banerji Biswadip¹,Iqbal Javed¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010981d

Reference26 articles.

1. Antiparallel Sheet Formation in β-Peptide Foldamers: Effects of β-Amino Acid Substitution on Conformational Preference1

2. N-α-benzoyl-cis-4-amino-L-proline: A γ-turn mimetic

3. Peptide backbone-to-backbone cyclisation as an avenue to β-turn mimics

4. Protein β-turn mimetics I. Design, synthesis, and evaluation in model cyclic peptides.

5. Conformationally constrained nonpeptide β-turn mimetics of enkephalin

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