Formal [3+2] Cycloaddition Between in situ Formed 1,4‐Benzodiazepin‐2‐One‐Based Azomethine Ylides and Azodicarboxylic Acid Derivatives: Diastereoselective Synthesis of Spiro‐1,4‐Benzodiazepin‐2‐Ones-Reference-Cited by-同舟云学术

Formal [3+2] Cycloaddition Between in situ Formed 1,4‐Benzodiazepin‐2‐One‐Based Azomethine Ylides and Azodicarboxylic Acid Derivatives: Diastereoselective Synthesis of Spiro‐1,4‐Benzodiazepin‐2‐Ones

Published:2021-01-20 Issue:5 Volume:363 Page:1379-1389
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Fan Xiao‐Zu¹,Wu Hui‐Hui¹,Tang Zhe¹,Zhang Heng¹,Cai Lu‐Yu¹,Bi Xiao‐Fan¹,Zhao Hong‐Wu¹^ORCID

Affiliation:

1. College of Life Science and Bio-engineering Beijing University of Technology Beijing 100124 People's Republic of China

Funder

Beijing Municipal Commission of Education

Natural Science Foundation of Beijing Municipality

Funding Project for Academic Human Resources Development in Institutions of Higher Learning under the Jurisdiction of Beijing Municipality

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202001486

Reference47 articles.

1. For selected reviews see:

2. Quantitative Structure-Activity Relationships of the Benzodiazepines. A Review and Reevaluation

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

4. Spiro-[4H-pyrroIo[1,2-a][1,4]benzodiazepine-4,4′-piperidine] Derivatives as Potential Nootropic Agents: A Simple One-Pot Synthesis

5. Integrated Ugi-Based Assembly of Functionally, Skeletally, and Stereochemically Diverse 1,4-Benzodiazepin-2-ones

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1. Catalytic Stereoselective Multicomponent Reactions for the Synthesis of Spiro Derivatives: Recent Progress;European Journal of Organic Chemistry;2022-12-08

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