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A synthetic approach to the mitosenes

โœ Scribed by J. Rebek Jr.; J.-C.E. fsGehret


Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
114 KB
Volume
18
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


Mitosenes, the chemical degradation products of the mitomycins, 1 are synthetically accessible through a number of approaches which build the pyrrolisidine system onto an existing 6membered ring.

2 We offer here an alternative, rapid assembly of the ring system, from which access to optically active mitosenes appears feasible. Our approach is based on Huisgen's 394 pyrrole synthesis formalized below; applied to the case at hand, a mUnchnone is generated from


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