Synthesis of D-homo analogs of neurosteroids

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17(13→18)-Abeo and D-homo analogs of the natural neurosteroid 3α-hydroxy-5αH-pregnan-20-one were prepared by anionic or radical (mercury (II) hydride mediated) rearrangements of steroidal cyclopropylketones respectively.

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Detalles Bibliográficos
Autores principales:	Di Chenna, P., Ghini, A.A., Burton, G.
Formato:	JOUR
Materias:	11alpha hydroxyprogesterone 3alpha hydroxy 5alpha pregnan 20 one derivative cyclopropylketone derivative dehydropregnenolone acetate ketone derivative mercury derivative neurosteroid derivative pregnenolone derivative steroid unclassified drug conference paper drug structure drug synthesis reaction analysis
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p447_DiChenna
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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