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1.
Chem Commun (Camb) ; (39): 5910-2, 2009 Oct 21.
Article in English | MEDLINE | ID: mdl-19787138

ABSTRACT

A new class of enantiopure carbene precursors based on cheap camphor has been developed, and a restricted rotation of one N-substituent due to the C-10 methyl group of the camphor skeleton has been found; in situ prepared corresponding carbenes revealed the same behaviour.

2.
Chem Commun (Camb) ; (9): 1040-2, 2009 Mar 07.
Article in English | MEDLINE | ID: mdl-19225629

ABSTRACT

Asymmetric imidazolinium-dithiocarboxylates have been found for the first time to be highly selective catalysts; in the present case, the novel organocatalysts were able to catalyze the Staudinger reaction in up to 96% ee and 99% yield.

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