Regio- and stereoselective synthesis of enantiomerically pure [60]fullerene tris-adducts with an inherently chiral e,e,e addition pattern

Chronakis N, Hirsch A (2005)


Publication Type: Journal article, Original article

Publication year: 2005

Journal

Original Authors: Chronakis N., Hirsch A.

Publisher: Royal Society of Chemistry

Pages Range: 3709-3711

Journal Issue: 29

DOI: 10.1039/b502822a

Abstract

The synthesis and flash column chromatographic separation of c enantiomerically pure tris-adducts of C with an e,e,e-addition pattern is achieved via cyclopropanation with chiral D-symmetrical cyclo-tris(malonate) tethers. © The Royal Society of Chemistry 2005.

Authors with CRIS profile

How to cite

APA:

Chronakis, N., & Hirsch, A. (2005). Regio- and stereoselective synthesis of enantiomerically pure [60]fullerene tris-adducts with an inherently chiral e,e,e addition pattern. Chemical Communications, 29, 3709-3711. https://dx.doi.org/10.1039/b502822a

MLA:

Chronakis, Nikos, and Andreas Hirsch. "Regio- and stereoselective synthesis of enantiomerically pure [60]fullerene tris-adducts with an inherently chiral e,e,e addition pattern." Chemical Communications 29 (2005): 3709-3711.

BibTeX: Download