α‐Boryl Isocyanides Enable Facile Preparation of Bioactive Boropeptides

Adam Zajdlik(University of Toronto), Zezhou Wang(University Health Network), Jennifer L. Hickey(University of Toronto), Asma M. Aman(Ontario Institute for Cancer Research), Aaron D. Schimmer(Princess Margaret Cancer Centre), Andrei K. Yudin(University of Toronto)
Angewandte Chemie International Edition
July 1, 2013
Cited by 81

Abstract

Entry to bioactive boropeptides: MIDA-containing α-boryl isocyanides are isolable molecules which allow one-step access to boroalkyl-functionalized heterocycles as well as biologically active boropeptides through a multicomponent approach. Among these derivatives are 6-boromorpholinones, novel borocycles with nanomolar IC50 values for 20S proteasome inhibition. MIDA=N-methyliminodiacetyl. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.


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