Nitroamine radicals as intermediates in the functionalization of non-activated carbon atoms

Photolysis of N-iodonitroamines generated in situ from the steroidal nitroamines 6β-nitroamino-5α-cholestan-3β-ol acetate, 6β-nitroamino-5α-cholestane-3β,5α-diol diacetate, and 20R-nitroaminopregn-5-en-3-ol acetate removes hydrogen atoms from the Me-18 and Me-19 groups to give 6β-,19-N-nitroepinino-5α-cholestan-3β-ol acetate, 6β,19-N-nitroepinino-5α-cholestane-3β5α-diol diacetate, and 18,20R-N-nitroepiminopregn-5-en-3β-ol acetate.

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Bibliographic Details
Main Authors: Hernández, Rosendo, Rivera, Augusto, Salazar, José A., Suárez, Ernesto
Other Authors: Ministerio de Asuntos Exteriores y Cooperación (España)
Format: artículo biblioteca
Language:English
Published: Royal Society of Chemistry (UK) 1980
Online Access:http://hdl.handle.net/10261/17572
http://dx.doi.org/10.13039/501100003767
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