Nafion-H mediated selective deprotection of terminal isopropylidene acetals and trityl ethers. Application in the synthesis of a substituted piperidone

Rawal, Girish K. ; Rani, Shikha ; Kumar, Amit ; Vankar, Yashwant D. (2006) Nafion-H mediated selective deprotection of terminal isopropylidene acetals and trityl ethers. Application in the synthesis of a substituted piperidone Tetrahedron Letters, 47 (51). pp. 9117-9120. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.10.067

Abstract

A facile chemoselective hydrolysis of terminal isopropylidene acetals has been achieved in good to excellent yields within 2-4 h using Nafion-H in methanol at ambient temperature. This procedure has been employed to synthesize a substituted piperidone derivative. Similarly, trityl ethers are also deprotected to the corresponding alcohols in excellent yields using Nafion-H at room temperature.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:58294
Deposited On:31 Aug 2011 06:39
Last Modified:31 Aug 2011 06:39

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