Issue 43, 2007

New chiral diamino-bis(tert-thiophene): an effective ligand for Pd- and Zn-catalyzed asymmetric transformations

Abstract

Enantiomerically pure diamino-bis(tert-thiophene) 1b proved to be a valuable and flexible chiral ligand for Pd- and Zn-catalyzed transformations, allowing for high levels of stereocontrol in asymmetric allylic alkylation (ee up to 99%) and hydrosilylations of prochiral carbonyls (ee up to 97%).

Graphical abstract: New chiral diamino-bis(tert-thiophene): an effective ligand for Pd- and Zn-catalyzed asymmetric transformations

Supplementary files

Article information

Article type
Communication
Submitted
01 Aug 2007
Accepted
14 Aug 2007
First published
21 Aug 2007

Chem. Commun., 2007, 4519-4521

New chiral diamino-bis(tert-thiophene): an effective ligand for Pd- and Zn-catalyzed asymmetric transformations

M. Bandini, M. Melucci, F. Piccinelli, R. Sinisi, S. Tommasi and A. Umani-Ronchi, Chem. Commun., 2007, 4519 DOI: 10.1039/B711666G

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