Synthesis of Benzodiazepine β-Turn Mimetics by an Ugi 4CC/Staudinger/Aza-Wittig Sequence. Solving the Conformational Behavior of the Ugi 4CC Adducts-Reference-Cited by-同舟云学术

Synthesis of Benzodiazepine β-Turn Mimetics by an Ugi 4CC/Staudinger/Aza-Wittig Sequence. Solving the Conformational Behavior of the Ugi 4CC Adducts

Published:2009-02-03 Issue:5 Volume:74 Page:2189-2192
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sañudo María¹,García-Valverde María¹,Marcaccini Stefano¹,Delgado Jacinto J.¹,Rojo Josefa¹,Torroba Tomás¹

Affiliation:

1. Departamento de Química, Facultad de Ciencias & Parque Científico Tecnológico, Universidad de Burgos, 09001 Burgos, Spain, and Dipartamento di Chimica Organica “Ugo Schiff”, Università di Firenze, via della Lastruccia 13, I-50121 Sesto Fiorentino (FI), Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8025862

Reference63 articles.

1. GABAA/Bz Receptor Subtypes as Targets for Selective Drugs

2. GABA-A receptors: a viable target for novel anxiolytics?

3. The benzodiazepine binding site of GABAAreceptors as a target for the development of novel anxiolytics

4. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

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