Journal article

Mimics of L-rhamnose: Analogues of rhamnopyranose containing a constituent alpha-amino acid at the anomeric position. A rhamnopyranose analogue of hydantocidin

Abstract:: Ionic brominative oxidation of 2-amino derivatives of protected heptonolactones derived from L-rhamnose provides a key bicyclic intermediate for the synthesis of analogues of L-rhamnopyranose with spirohydantoins and spirodiketopiperazines at the anomeric position; the same intermediate can be used for the synthesis of novel glycopeptides containing a constituent rhamnopyranose amino acid. such materials may allow an approach to new studies of diseases induced by mycobacteria, such as tuberculosis and leprosy.

Publication status:: Published

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APA Style

Estevez, J., Smith, M., Wormald, M. R., Besra, G., Brennan, P., Nash, R., & Fleet, G. (1996). Mimics of L-rhamnose: Analogues of rhamnopyranose containing a constituent alpha-amino acid at the anomeric position. A rhamnopyranose analogue of hydantocidin. TETRAHEDRON-ASYMMETRY, 7(2), 391–394.

MLA Style

Estevez, J, et al. “Mimics of L-Rhamnose: Analogues of Rhamnopyranose Containing a Constituent Alpha-Amino Acid at the Anomeric Position. A Rhamnopyranose Analogue of Hydantocidin.” TETRAHEDRON-ASYMMETRY, vol. 7, no. 2, 1996, pp. 391–94.

Chicago Style

Estevez, J, M Smith, MR Wormald, et al. 1996. “Mimics of L-Rhamnose: Analogues of Rhamnopyranose Containing a Constituent Alpha-Amino Acid at the Anomeric Position. A Rhamnopyranose Analogue of Hydantocidin.” TETRAHEDRON-ASYMMETRY 7 (2): 391–94.
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Publisher copy:: 10.1016/0957-4166(96)00014-6

Authors

+ Estevez, J More by this author

Role:: Author

+ Smith, M More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Wormald, MR More by this author

Role:: Author

+ Besra, G More by this author

Role:: Author

+ Brennan, P More by this author

Role:: Author

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Journal:: TETRAHEDRON-ASYMMETRY More from this journal
Volume:: 7
Issue:: 2
Pages:: 391-394
Publication date:: 1996-02-01
DOI:: 10.1016/0957-4166(96)00014-6
ISSN:: 0957-4166

Pubs id:: pubs:45086
UUID:: uuid:ef396526-8991-4db0-b69c-2a90826b2ce1
Local pid:: pubs:45086
Source identifiers:: 45086
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_ef39652689914db0b69c2a90826b2ce1

Terms of use

Copyright date:: 1996

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

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