Tetrahedron Letters p. 6949 - 6952 (1995)
Update date:2022-08-16
Topics:
Merchan, Francisco L.
Merino, Pedro
Tejero, Tomas
An exploration of the diastereoselective addition of cyanide reagents to the nitrone 1 derived from D-glyceraldehyde acetonide to afford mixtures of syn-2 and anti-2 is presented. Trimethylsilyl cyanide was found to add to the nitrone 1 with essentially complete syn-stereoselectivity in excellent yields.
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