Syntheses of lamellarins I and K by [3+2] cycloaddition of a nitrone to an alkyne
Lamellarins I and K were obtained by a new approach based on the 1,3-dipolar cycloaddition of a nitrone to an alkyne. The key cycloaddition yields an isoxazoline which rearranges to afford the central pyrrole ring.
Díaz,Guitián,Castedo
p. 1164 - 1166
(2007/10/03)
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