Journal article
Equilibration in bicyclic pyroglutamates by ring opening-reclosure
- Abstract:
- Enantiopure bicyclic tetramates, readily obtained by Dieckmann ring closure on oxazolidine-derived templates, can be further converted to hydroxypyroglutamates by kinetically controlled nucleophilic additions, and some of these products are capable of equilibration via a facile retro-aldol/aldol reclosure. © 2008 Elsevier Ltd. All rights reserved.
- Publication status:
- Published
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Authors
- Journal:
- TETRAHEDRON LETTERS More from this journal
- Volume:
- 49
- Issue:
- 43
- Pages:
- 6202-6204
- Publication date:
- 2008-10-20
- DOI:
- ISSN:
-
0040-4039
- Language:
-
English
- Pubs id:
-
pubs:40914
- UUID:
-
uuid:4723f32e-14b1-4269-b893-ab69a2bf18ee
- Local pid:
-
pubs:40914
- Source identifiers:
-
40914
- Deposit date:
-
2012-12-19
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- Copyright date:
- 2008
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