cheminform abstract: exopericyclic stereocontrol in johnson—claisen rearrangements of allylic...

ChemInform 2011, 42, issue 01 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Stereochemistry O 0030 DOI: 10.1002/chin.201104021 Exopericyclic Stereocontrol in Johnson—Claisen Rearrangements of Allylic Sul- fides. — The selectivity of the Johnson—Claisen rearrangement of allylic sulfides is highly dependent on the allylic substitution pattern. — (CRAIG*, D.; HARVEY, J. W.; O'BRIEN, A. G.; WHITE, A. J. P.; Chem. Commun. (Cambridge) 46 (2010) 37, 6932-6934, http://dx.doi.org/10.1039/c0cc01039a ; Dep. Chem., Imp. Coll., London SW7 2AZ, UK; Eng.) — D. Singer 04- 021

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Page 1: ChemInform Abstract: Exopericyclic Stereocontrol in Johnson—Claisen Rearrangements of Allylic Sulfides

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StereochemistryO 0030 DOI: 10.1002/chin.201104021

Exopericyclic Stereocontrol in Johnson—Claisen Rearrangements of Allylic Sul-fides. — The selectivity of the Johnson—Claisen rearrangement of allylic sulfides is highly dependent on the allylic substitution pattern. — (CRAIG*, D.; HARVEY, J. W.; O'BRIEN, A. G.; WHITE, A. J. P.; Chem. Commun. (Cambridge) 46 (2010) 37, 6932-6934, http://dx.doi.org/10.1039/c0cc01039a ; Dep. Chem., Imp. Coll., London SW7 2AZ, UK; Eng.) — D. Singer

04- 021

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