A new facile synthesis of steroid dimers containing 17,17′-dicarboxamide spacers
01 natural sciences
0104 chemical sciences
3. Good health
DOI:
10.1016/j.tetlet.2013.02.108
Publication Date:
2013-03-21T03:16:37Z
AUTHORS (5)
ABSTRACT
Abstract A set of new steroid dimers linked through ring D–ring D were synthesized via catalytic diaminocarbonylation of 17-iodo-5α-androst-16-ene, in the presence of palladium–phosphine in situ catalysts and aliphatic or aromatic diamines as N -nucleophiles. The dimeric steroidal compounds containing 17,17′-dicarboxamide spacers were obtained through highly chemoselective reactions in good isolated yields and completely characterized by spectroscopic techniques.
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