1,4-Additions to γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones: Synthesis of Highly Functionalized Amino Acid Derivatives-Reference-Cited by-同舟云学术

1,4-Additions to γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones: Synthesis of Highly Functionalized Amino Acid Derivatives

Published:1999-06-29 Issue:3 Volume:1 Page:481-484
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Steurer Steffen¹,Podlech Joachim¹

Affiliation:

1. Institut für Organische Chemie der Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol990672y

Reference29 articles.

1. (a) Fischer, N. H.; Olivier, E. J.; Fischer, H. D. InProgress in the Chemistry ofOrganic Natural Products; Herz, W., Grisebach, H., Kirby, G. W., Eds.; Springer: Wien, 1979; Vol. 38, p 47.

2. Synthesis and Biological Activity of ?-Methylene-?-butyrolactones

3. Renin inhibitors based on dipeptide analogs. Incorporation of the hydroxyethylene isostere at the P2/P3 sites

4. Renin inhibitors containing new P1-P1' dipeptide mimetics with heterocycles in P1'

5. Dipeptide isosteres. 2. Synthesis of hydroxyethylene dipeptide isostere diastereomers from a common γ-lactone intermediate. Preparation of renin and HIV-1 protease inhibitor transition state mimics.

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