- Abstract:
- Efficient SN2 ring closure of open chain trihydroxytriflates-in which the leaving group is on a primary carbon adjacent to a quaternary centre-provides access to tetrahydrofurans with branched carbon chains from branched carbohydrate lactones; the first examples of a new class of branched chain tetrahydrofuran α,α-disubstituted-δ-sugar amino acid scaffolds are described. © 2005 Elsevier Ltd. All rights reserved.
- Publication status:
- Published
- Publisher copy:
- 10.1016/j.tetlet.2005.06.029
-
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- Journal:
- TETRAHEDRON LETTERS
- Volume:
- 46
- Issue:
- 34
- Pages:
- 5761-5765
- Publication date:
- 2005-08-22
- DOI:
- ISSN:
-
0040-4039
- URN:
-
uuid:644ecf70-caa7-407f-a95c-441357ddae6c
- Source identifiers:
-
39582
- Local pid:
- pubs:39582
- Language:
- English
- Copyright date:
- 2005
Journal article
Branched tetrahydrofuran alpha,alpha-disubstituted-delta-sugar amino acid scaffolds from branched sugar lactones: a new family of foldamers?
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