Journal article

THE SYNTHESIS FROM D-XYLOSE OF THE POTENT AND SPECIFIC ENANTIOMERIC GLUCOSIDASE INHIBITORS, 1,4-DIDEOXY-1,4-IMINO-D-ARABINITOL AND 1,4-DIDEOXY-1,4-IMINO-L-ARABINITOL

Abstract:: Both enantiomers of 1,4-dideoxy-1,4-iminoarabinitol are specific inhibitors of glucosidases. The synthesis of 1,4-dideoxy-1,4-imino-D-arabinitol involves connecting C2 and C5 of xylose together with nitrogen, whereas the synthesis of 1,4-dideoxy-1.4-imino-L-arabinitol requires C1 and C4 of xylose to be joined together by nitrogen. 1,4-Dideoxy-1,4-imino-D-arabinitol is a naturally occurring pyrrolidine alkaloid found in Arachniodes standishii and Angylocalyx boutiqueanus. © 1986.

Publication status:: Published

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APA Style

Fleet, G., & Smith, P. (1986). THE SYNTHESIS FROM D-XYLOSE OF THE POTENT AND SPECIFIC ENANTIOMERIC GLUCOSIDASE INHIBITORS, 1,4-DIDEOXY-1,4-IMINO-D-ARABINITOL AND 1,4-DIDEOXY-1,4-IMINO-L-ARABINITOL. TETRAHEDRON, 42(20), 5685–5692.

MLA Style

Fleet, G., and P. Smith. “THE SYNTHESIS FROM D-XYLOSE OF THE POTENT AND SPECIFIC ENANTIOMERIC GLUCOSIDASE INHIBITORS, 1,4-DIDEOXY-1,4-IMINO-D-ARABINITOL AND 1,4-DIDEOXY-1,4-IMINO-L-ARABINITOL.” TETRAHEDRON, vol. 42, no. 20, 1986, pp. 5685–92.

Chicago Style

Fleet, G, and P Smith. 1986. “THE SYNTHESIS FROM D-XYLOSE OF THE POTENT AND SPECIFIC ENANTIOMERIC GLUCOSIDASE INHIBITORS, 1,4-DIDEOXY-1,4-IMINO-D-ARABINITOL AND 1,4-DIDEOXY-1,4-IMINO-L-ARABINITOL.” TETRAHEDRON 42 (20): 5685–92.
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Publisher copy:: 10.1016/S0040-4020(01)88174-6

Authors

+ Fleet, G More by this author

Role:: Author

+ Smith, P More by this author

Role:: Author

Journal:: TETRAHEDRON More from this journal
Volume:: 42
Issue:: 20
Pages:: 5685-5692
Publication date:: 1986-01-01
DOI:: 10.1016/S0040-4020(01)88174-6
ISSN:: 0040-4020

Language:: English
Pubs id:: pubs:42663
UUID:: uuid:bc64fd3a-ee53-41c2-bbfd-95f285093467
Local pid:: pubs:42663
Source identifiers:: 42663
Deposit date:: 2012-12-19

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Copyright date:: 1986

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

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