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Integrated Ugi-Based Assembly of Functionally, Skeletally, and Stereochemically Diverse 1,4-Benzodiazepin-2-ones
A practical, integrated and versatile U-4CR-based assembly of 1,4-benzodiazepin-2-ones exhibiting functionally, skeletally, and stereochemically diverse substitution patterns is described. By virtue of its convergence, atom economy, and bond-forming efficiency, the methodology documented herein exem...
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Published in: | Journal of organic chemistry 2015-02, Vol.80 (3), p.1533-1549 |
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Main Authors: | , , , , , , , , , |
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container_end_page | 1549 |
container_issue | 3 |
container_start_page | 1533 |
container_title | Journal of organic chemistry |
container_volume | 80 |
creator | Azuaje, Jhonny Pérez-Rubio, José M Yaziji, Vicente El Maatougui, Abdelaziz González-Gomez, José Carlos Sánchez-Pedregal, Vı́ctor M Navarro-Vázquez, Armando Masaguer, Christian F Teijeira, Marta Sotelo, Eddy |
description | A practical, integrated and versatile U-4CR-based assembly of 1,4-benzodiazepin-2-ones exhibiting functionally, skeletally, and stereochemically diverse substitution patterns is described. By virtue of its convergence, atom economy, and bond-forming efficiency, the methodology documented herein exemplifies the reconciliation of structural complexity and experimental simplicity in the context of medicinal chemistry projects. |
doi_str_mv | 10.1021/jo502382q |
format | article |
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language | eng |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Benzodiazepinones - chemistry Combinatorial Chemistry Techniques Molecular Structure Organic Chemistry Phenomena Stereoisomerism |
title | Integrated Ugi-Based Assembly of Functionally, Skeletally, and Stereochemically Diverse 1,4-Benzodiazepin-2-ones |
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