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

Journal Article


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Abstract


  • The synthesis of two new trihydroxylated pyrrolidines, in a highly diastereoselective manner, has been developed using the Meyer-Schuster rearrangement as a key step. © 2011 Taylor & Francis Group, LLC.

UOW Authors


Publication Date


  • 2011

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.

Scopus Eid


  • 2-s2.0-79958864875

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=7424&context=scipapers

Ro Metadata Url


  • http://ro.uow.edu.au/scipapers/4082

Number Of Pages


  • 10

Start Page


  • 2435

End Page


  • 2445

Volume


  • 41

Issue


  • 16

Abstract


  • The synthesis of two new trihydroxylated pyrrolidines, in a highly diastereoselective manner, has been developed using the Meyer-Schuster rearrangement as a key step. © 2011 Taylor & Francis Group, LLC.

UOW Authors


Publication Date


  • 2011

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.

Scopus Eid


  • 2-s2.0-79958864875

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=7424&context=scipapers

Ro Metadata Url


  • http://ro.uow.edu.au/scipapers/4082

Number Of Pages


  • 10

Start Page


  • 2435

End Page


  • 2445

Volume


  • 41

Issue


  • 16