Palladium/Lewis Acid Co-catalyzed Divergent Asymmetric
Ring-Opening Reactions of Azabenzonorbornadienes with Alcohols

Fan, Baomin

Palladium/Lewis Acid Co-catalyzed Divergent Asymmetric Ring-Opening Reactions of Azabenzonorbornadienes with Alcohols

Version 2 2016-10-03, 15:28

Version 1 2016-09-28, 16:07

Posted on 2016-09-28 - 00:00

By fine tuning the combinations of chiral palladium catalysts and Lewis acids, both the additional and reductive asymmetric ring-opening reactions of azabenzonorbornadienes with alcohols were accomplished with good chemoselectivity, regioselectivity, and enantioselectivity. It was proven that the reductive ring-opening products were generated through a transfer-hydrogenation process with alcohols as hydrogen source.

CITE THIS COLLECTION

DataCite

3 Biotech

3D Printing in Medicine

3D Research

3D-Printed Materials and Systems

4OR

AAPG Bulletin

AAPS Open

AAPS PharmSciTech

Abhandlungen aus dem Mathematischen Seminar der Universität Hamburg

ABI Technik (German)

Academic Medicine

Academic Pediatrics

Academic Psychiatry

Academic Questions

Academy of Management Discoveries

Academy of Management Journal

Academy of Management Learning and Education

Academy of Management Perspectives

Academy of Management Proceedings

Academy of Management Review

Yang, Fan; Chen, Jingchao; Xu, Jianbin; Ma, Fujie; Zhou, Yongyun; Shinde, Madhuri Vikas; et al. (2016). Palladium/Lewis Acid Co-catalyzed Divergent Asymmetric Ring-Opening Reactions of Azabenzonorbornadienes with Alcohols. ACS Publications. Collection. https://doi.org/10.1021/acs.orglett.6b02300

https://doi.org/10.1021/acs.orglett.6b02300

or

Select your citation style and then place your mouse over the citation text to select it.