Journal article

SYNTHESIS OF THE POTENT ANTIVIRAL OXETANE NUCLEOSIDE EPINOROXETANOCIN FROM D-LYXONOLACTONE

Abstract:: A short synthesis of epinoroxetanocin [9-(β-D-threo-oxetanosyl)adenine], free from its α-anomer, from D-lyxonolactone is described. The X-ray crystal structure of a benzylidene-protected derivative of epinoroxetanocin is reported. A comparison of the in vitro activity against HIV-1 of oxetanocin, noroxetanocin and epinoroxetanocin as anti-viral agents is given. © 1990.

Publication status:: Published

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APA Style

Wang, Y., Fleet, G., Storer, R., Myers, P., Wallis, C., Doherty, O., Watkin, D., Vogt, K., Witty, D., Wilson, F., & Peach, J. (1990). SYNTHESIS OF THE POTENT ANTIVIRAL OXETANE NUCLEOSIDE EPINOROXETANOCIN FROM D-LYXONOLACTONE. TETRAHEDRON-ASYMMETRY, 1(8), 527–530.

MLA Style

Wang, Y, et al. “SYNTHESIS OF THE POTENT ANTIVIRAL OXETANE NUCLEOSIDE EPINOROXETANOCIN FROM D-LYXONOLACTONE.” TETRAHEDRON-ASYMMETRY, vol. 1, no. 8, 1990, pp. 527–30.

Chicago Style

Wang, Y, G Fleet, R Storer, et al. 1990. “SYNTHESIS OF THE POTENT ANTIVIRAL OXETANE NUCLEOSIDE EPINOROXETANOCIN FROM D-LYXONOLACTONE.” TETRAHEDRON-ASYMMETRY 1 (8): 527–30.
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Publisher copy:: 10.1016/S0957-4166(00)80541-8

Authors

+ Wang, Y More by this author

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+ Fleet, G More by this author

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+ Storer, R More by this author

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+ Myers, P More by this author

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+ Wallis, C More by this author

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Journal:: TETRAHEDRON-ASYMMETRY More from this journal
Volume:: 1
Issue:: 8
Pages:: 527-530
Publication date:: 1990-01-01
DOI:: 10.1016/S0957-4166(00)80541-8
EISSN:: 1362-511X
ISSN:: 0957-4166

Language:: English
Pubs id:: pubs:43339
UUID:: uuid:18cbef90-abf2-48f3-982e-23d6f43081a6
Local pid:: pubs:43339
Source identifiers:: 43339
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_18cbef90abf248f3982e23d6f43081a6

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Copyright date:: 1990

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

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