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Stereoselective synthesis of two new trihydroxylated pyrrolidines using a meyer-schuster rearrangement

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posted on 2024-11-14, 14:56 authored by Nalivela K Swamy, Stephen PyneStephen Pyne
The synthesis of two new trihydroxylated pyrrolidines, in a highly diastereoselective manner, has been developed using the Meyer-Schuster rearrangement as a key step. C 2011 Taylor & Francis Group, LLC.

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Citation

Swamy, N. Kumara. & Pyne, S. G. (2011). Stereoselective synthesis of two new trihydroxylated pyrrolidines using a meyer-schuster rearrangement. Synthetic Communications, 41 (16), 2435-2445.

Journal title

Synthetic Communications

Volume

41

Issue

16

Pagination

2435-2445

Publisher website/DOI

Language

English

RIS ID

42456

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    StereoselectivesynthesistwotrihydroxylatedpyrrolidinesusingmeyerschusterrearrangementCMMB

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