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The "Triamino-analogue" of Methyl Cholate; A Practical, Large-Scale Synthesis
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The "Triamino-analogue" of Methyl Cholate; A Practical, Large-Scale Synthesis
The "Triamino-analogue" of Methyl Cholate; A Practical, Large-Scale Synthesis
Anthony P. Davis
Anthony P. Davis
MP
M. Nieves Pérez-Payán
M. Nieves Pérez-Payán
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8 June 1999
journal article
letter
Published by
Georg Thieme Verlag KG
in
Synlett
Vol. 1999
(Sup. 1)
,
991-993
https://doi.org/10.1055/s-1999-3114
Abstract
The triamino steroids
2
are in demand as facial amphiphiles and starting materials for supramolecular chemistry.
2
(R = Me) is now available from cholic acid
1
in substantial quantities via a new, high-yielding procedure.
Keywords
BILE ACIDS
SCAFFOLD
SUPRAMOLECULAR CHEMISTRY
FACIAL AMPHIPHILE
OXIME REDUCTION
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Cited by 30 articles