Journal article

Asymmetric synthesis of (+)-negamycin

Abstract:: (+)-Negamycin was synthesised employing the highly diastereoselective conjugate addition of lithium (α-methylbenzyl)benzylamide in the key step. The synthesis was completed in 13 steps starting from ethyl 4-chloroacetoacetate with an overall yield of 24%.

Publication status:: Published

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APA Style

Davies, S., & Ichihara, O. (1996). Asymmetric synthesis of (+)-negamycin. TETRAHEDRON-ASYMMETRY, 7(7), 1919–1922.

MLA Style

Davies, S, and O Ichihara. “Asymmetric Synthesis of (+)-Negamycin.” TETRAHEDRON-ASYMMETRY, vol. 7, no. 7, 1996, pp. 1919–22.

Chicago Style

Davies, S, and O Ichihara. 1996. “Asymmetric Synthesis of (+)-Negamycin.” TETRAHEDRON-ASYMMETRY 7 (7): 1919–22.
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Publisher copy:: 10.1016/0957-4166(96)00230-3

Authors

+ Davies, S More by this author

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

+ Ichihara, O More by this author

Role:: Author

Journal:: TETRAHEDRON-ASYMMETRY More from this journal
Volume:: 7
Issue:: 7
Pages:: 1919-1922
Publication date:: 1996-07-01
DOI:: 10.1016/0957-4166(96)00230-3
ISSN:: 0957-4166

Pubs id:: pubs:110841
UUID:: uuid:1f49aab1-ff87-4a10-9862-2549ba9a7666
Local pid:: pubs:110841
Source identifiers:: 110841
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_1f49aab1ff874a1098622549ba9a7666

Terms of use

Copyright date:: 1996

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

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