## FFfm A Mitsunobu type of coupling is used to prepare a complex phenyl a y ether which undergoes a Claisen rearrangement. A synthetic route to a mitosene is achieved.
โฆ LIBER โฆ
A synthetic approach to the mitosenes
โ 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
No coin nor oath required. For personal study only.
โฆ 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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