885104-48-3Relevant academic research and scientific papers
TMSOTf mediated '5/6-: Endo-dig ' reductive hydroamination for the stereoselective synthesis of pyrrolidine and piperidine derivatives
Gharpure, Santosh J.,Vishwakarma, Dharmendra S.,Patel, Raj K.
, p. 6858 - 6861 (2019)
A TMSOTf mediated 5/6-endo-dig reductive hydroamination cascade on internal alkynylamines gave expedient, stereoselective access to pyrrolidine and piperidine derivatives. We also demonstrate that a protecting group on nitrogen has a profound effect on the reactivity as well as diastereoselectivity of the reductive hydroamination cascade.
NOVEL B1 BRADYKININ RECEPTOR ANTAGONISTS
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Page/Page column 51; 53, (2010/11/08)
The invention encompasses novel compounds of a formula I and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for treatment of diseases mediated by B1 bradykinin receptor.
