Conformational Study and Enantioselective, Regiospecific Syntheses of Novel Aminoxy trans-Proline Analogues Derived from an Acylnitroso Diels−Alder Cycloaddition-Reference-Cited by-同舟云学术

Conformational Study and Enantioselective, Regiospecific Syntheses of Novel Aminoxy trans-Proline Analogues Derived from an Acylnitroso Diels−Alder Cycloaddition

Published:2001-08-08 Issue:18 Volume:66 Page:6046-6056
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shireman Brock T.¹,Miller Marvin J.¹,Jonas Marco¹,Wiest Olaf¹

Affiliation:

1. Department of Chemistry & Biochemistry, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, Indiana 46556-5670

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010284l

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4. β-Peptide Foldamers: Robust Helix Formation in a New Family of β-Amino Acid Oligomers

5. Formation of Short, Stable Helices in Aqueous Solution by β-Amino Acid Hexamers

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