Synthesis and conformational studies of α/β2,3-peptides derived from alternating β2,3-amino acids and l-Ala repeats-Reference-Cited by-同舟云学术

Synthesis and conformational studies of α/β2,3-peptides derived from alternating β2,3-amino acids and l-Ala repeats

Published:2015 Issue:5 Volume:39 Page:3295-3309
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Sharma Gangavaram V. M.¹²³⁴,Sridhar Tailor¹²³⁴,Veena Bacchu¹²³⁴,Purushotham Reddy Pothula⁵²³⁴,Reddy Sheri Venkata¹²³⁴,Bruneau Christian⁶⁷,Kunwar Ajit C.⁵²³⁴

Affiliation:

1. Organic and Biomolecular Chemistry Division

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad 500 007

4. India

5. Centre for Nuclear Magnetic Resonance and Structural Chemistry

6. UMR6226: Institut des Sciences Chimiques de Rennes

7. France

Abstract

A new class of α/β^2,3-peptides were synthesized from C-linked carbo-β^2,3-amino acids (β^2,3-Caas) and investigated to understand the impact of the side chains (allyl/propargyl) at the Cα-position on their conformations.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C4NJ02031F

Reference60 articles.

1. A Field Guide to Foldamers

2. Design of Folded Peptides

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