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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 1
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Original Articles

One-Pot Mitsunobu-Staudinger Preparation of 3-Aminocholan-24-oic Acid Esters from 3-Hydroxycholan-24-oic Acid Esters

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Pages 109-117 | Received 26 Jun 1997, Published online: 20 Aug 2006
 

Abstract

3-Hydroxycholan-24-oic acid esters are easily converted into the corresponding 3-amino derivatives via Mitsunobu reaction with diphenylphosphoryl azide (DPPA) and Staudinger reduction with PPh3/H2O of the intermediate azido compound in THF.

Notes

DTPA = diethylenetriaminopentaacetic acid

DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraaceticacid

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