Synthesis of Enantiomerically Pure 1,2-Diamine Derivatives of 7-Azabicyclo[2.2.1]heptane. New Leads as Glycosidase Inhibitors and Rigid Scaffolds for the Preparation of Peptide Analogues-Reference-Cited by-同舟云学术

Synthesis of Enantiomerically Pure 1,2-Diamine Derivatives of 7-Azabicyclo[2.2.1]heptane. New Leads as Glycosidase Inhibitors and Rigid Scaffolds for the Preparation of Peptide Analogues

Published:2003-06-10 Issue:14 Volume:68 Page:5632-5640
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Moreno-Vargas Antonio J.¹,Schütz Catherine¹,Scopelliti Rosario¹,Vogel Pierre¹

Affiliation:

1. Institut de Chimie Moléculaire et Biologique de l'Ecole Polytechnique Fédérale de Lausanne, EPFL-BCH, CH-1015 Lausanne-Dorigny, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0301088

Reference63 articles.

1. Derivatives of (2R,3R,4S)-2-Aminomethylpyrrolidine-3,4-diol are selective α-Mannosidase inhibitors

2. Strategies for the Dynamic Integration of Combinatorial Synthesis and Screening

3. Dynamic Combinatorial Chemistry and Virtual Combinatorial Libraries

4. Imine exchange inO-aryl andO-alkyl oximes as a base reaction for aqueous ‘dynamic’ combinatorial libraries. A kinetic and thermodynamic study

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