Absolute configuration-dependent epoxide formation from isoflavan-4-ol stereoisomers by biphenyl dioxygenase of Pseudomonas pseudoalcaligenes strain KF707-Reference-Cited by-同舟云学术

Absolute configuration-dependent epoxide formation from isoflavan-4-ol stereoisomers by biphenyl dioxygenase of Pseudomonas pseudoalcaligenes strain KF707

Published:2010-11-10 Issue:6 Volume:89 Page:1773-1782
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

Seo Jiyoung,Kang Su-Il,Won Dongho,Kim Mihyang,Ryu Ji-Young,Kang Suk-Woo,Um Byung-Hun,Pan Cheol-Ho,Ahn Joong-Hoon,Chong Youhoon,Kanaly Robert A.,Han Jaehong,Hur Hor-Gil

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s00253-010-2989-1.pdf

Reference25 articles.

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3. Dewick MP, Harborne JB (1994) The flavonoids, advances in research since 1986. Chapman and Hall, London

4. Engler TA, LaTessa KO, Iyengar R, Chai W, Agrios K (1996) Stereoselectivity syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues. Bioorg Med Chem 4:1755–1769

5. Furukawa K, Hirose J, Hayashida S, Nakamura K (1994) Efficient degradation of trichlorothylene by a hybrid aromatic ring dioxygenase. J Bacteriol 176:2121–2123

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