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Synthesis and biological evaluation of a conformationally free seco-analogue of the immunosuppressant FR901483.

作者信息

Bonjoch J, Diaba F, Puigbó G, Solé D, Segarra V, Santamaría L, Beleta J, Ryder H, Palacios J M

机构信息

Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona, Spain.

出版信息

Bioorg Med Chem. 1999 Dec;7(12):2891-7. doi: 10.1016/s0968-0896(99)00250-3.

Abstract

The synthesis of an azaspirocyclic analogue of FR901483, phosphate 2, is described based on the implementation of a key 5-endo aminocyclization promoted by iodine for direct functionalization of the 1-azaspiro[4.5]decane ring at the C-3 atom. Compound 2 has no inhibitory activity in the cell proliferation assays reported.

摘要

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