Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Mondal, Rumpa
dc.contributor.author Venkaiah, Chintalapudi
dc.date.accessioned 2022-03-27T09:40:55Z
dc.date.available 2022-03-27T09:40:55Z
dc.date.issued 2010-06-01
dc.description.abstract A general process for the synthesis of substituted indenes and 1,2,3-triazoles was achieved, for the first time through a multicatalysis cascade reaction of 2-ethynylbenzaldehydes, CH acids, organic hydrides, and azides in the presence of a catalytic amount of L-proline/CuI/DIPEA. In this communication, we discovered the utilization of a single copper catalyst for two different reactions and shown synthetic application to the high-yielding synthesis of glucocorticoid receptor modulators. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation European Journal of Organic Chemistry
dc.identifier.issn 1434193X
dc.identifier.uri 10.1002/ejoc.201000220
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/ejoc.201000220
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13191
dc.subject Amino acids
dc.subject Carbocycles
dc.subject Domino reactions
dc.subject Heterocycles
dc.subject Organocatalysis
dc.title Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions
dc.type Journal. Article
dspace.entity.type
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