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Journal article

ANOMERIC SPIROHYDANTOINS OF MANNOFURANOSE - APPROACHES TO NOVEL ANOMERIC AMINO-ACIDS BY AN OXIDATIVE RING CONTRACTION

Abstract:: Bromine-induced oxidative ring contraction of an α-amino-δ-lactone gave a mixture of α-aminotetrahydrofurancarboxylic esters which may allow the preparation of stable amino acid derivatives at the anomeric position of mannofuranose. The synthesis of N-phenylhydantoins at the anomeric position of mannofuranose is reported. © 1993.

Publication status:: Published

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APA Style

Burton, J., Son, J., Fairbanks, A., Choi, S., Taylor, H., Watkin, D., Winchester, B., & Fleet, G. (1993). ANOMERIC SPIROHYDANTOINS OF MANNOFURANOSE - APPROACHES TO NOVEL ANOMERIC AMINO-ACIDS BY AN OXIDATIVE RING CONTRACTION. TETRAHEDRON LETTERS, 34(38), 6119–6122.

MLA Style

Burton, J., et al. “ANOMERIC SPIROHYDANTOINS OF MANNOFURANOSE - APPROACHES TO NOVEL ANOMERIC AMINO-ACIDS BY AN OXIDATIVE RING CONTRACTION.” TETRAHEDRON LETTERS, vol. 34, no. 38, 1993, pp. 6119–22.

Chicago Style

Burton, J, J Son, A Fairbanks, S Choi, H Taylor, D Watkin, B Winchester, and G Fleet. 1993. “ANOMERIC SPIROHYDANTOINS OF MANNOFURANOSE - APPROACHES TO NOVEL ANOMERIC AMINO-ACIDS BY AN OXIDATIVE RING CONTRACTION.” TETRAHEDRON LETTERS 34 (38): 6119–22.
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Publisher copy:: 10.1016/S0040-4039(00)61745-8

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+ Burton, J More by this author

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+ Son, J More by this author

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+ Fairbanks, A More by this author

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+ Choi, S More by this author

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+ Taylor, H More by this author

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Bibliographic Details

Journal:: TETRAHEDRON LETTERS
Volume:: 34
Issue:: 38
Pages:: 6119-6122
Publication date:: 1993-09-17
DOI:: 10.1016/S0040-4039(00)61745-8
ISSN:: 0040-4039

Item Description

Language:: English
Pubs id:: pubs:44264
UUID:: uuid:3a06e009-83a0-4fcb-9e4b-5d26d120d5d4
Local pid:: pubs:44264
Source identifiers:: 44264
Deposit date:: 2012-12-19

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Copyright date:: 1993

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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