PADAM reactions of α-aminoaldehydes: Identity of major and minor diastereomers from the Passerini reaction-Reference-Cited by-同舟云学术

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PADAM reactions of α-aminoaldehydes: Identity of major and minor diastereomers from the Passerini reaction

Published:2018-06 Issue:24 Volume:74 Page:2925-2941
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Zimuwandeyi Memory,Kola Fatima,Lemmerer Andreas,Brady Dean,Rousseau Amanda L.,Bode Moira L.

Funder

University of the Witwatersrand, Johannesburg

Department of Science and Technology, Republic of South Africa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Synthesis, Reactions and Uses of Isocyanides in Organic Synthesis. An Update

2. Passerini multicomponent reaction of protected α-aminoaldehydes as a tool for combinatorial synthesis of enzyme inhibitors

3. Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin A via a novel Passerini reaction–deprotection–acyl migration strategy

4. Facile and rapid route for the synthesis of novel norstatine analogs via PADAM-cyclization methodology

5. Short synthesis of protease inhibitors via modified Passerini condensation of N-Boc-α-aminoaldehydes

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1. The 100 facets of the Passerini reaction;Chemical Science;2021

2. Cyanoamidine Cyclization Approach to Remdesivir’s Nucleobase;Organic Letters;2020-10-21

3. Synthesis of highly functionalised 5-membered ring fused pyrimidine derivatives using an isocyanide-based one-pot, three component reaction;Tetrahedron Letters;2020-04

4. Diastereoselectivity in Passerini Reactions of Chiral Aldehydes and in Ugi Reactions of Chiral Cyclic Imines;European Journal of Organic Chemistry;2020-03-10

5. Stereodivergent access to all four stereoisomers of chiral tetrahydrobenzo[f][1,4]oxazepines, through highly diastereoselective multicomponent Ugi–Joullié reaction;RSC Advances;2020

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