Diastereoselection in the formation of spirocyclic oxindoles by the intramolecular heck reaction
Diastereoselective double Heck cyclizations of cyclohexene diamides 1 and 3 form contiguous quaternary stereocenters, with diastereoselection being controlled by the trans-diol protecting group. In this, the first in a series of two papers, the origin of
Overman, Larry E.,Watson, Donald A.
p. 2587 - 2599
(2007/10/03)
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