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Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition

CITE Title : Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition Personal Author(s) : Sato, Michio;Yagishita, Fumitoshi;Mino, Takashi;Uchiyama, Nahoko;Patel, Ashay;Chooi, Yit-Heng;Goda, Yukihiro;Xu, Wei;Noguchi, Hiroshi;Yamamoto, Tsuyoshi;Hotta, Kinya;Houk, Kendall N.;Tang, Yi;Watanabe, Kenji; Published Date : 11 2 2015;11-2-; Source : Chembiochem. 16(16):2294-2298 URL : https://stacks.cdc.gov/view/cdc/40002 Sato, Michio et al. (2015). Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition. 16(16). Sato, Michio et al. "Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition" 16, no. 16 (2015) Sato, Michio et al. "Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition" vol. 16, no. 16, 2015 Export RIS Citation Information.

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Sato, Michio ;

Yagishita, Fumitoshi

11 2 2015 | Chembiochem. 16(16):2294-2298

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Understanding enzymatic Diels-Alder (DA) reactions that can form complex natural product scaffolds is of considerable interest. Sch 210972 1, a potent...
A Carbonate-Forming Baeyer-Villiger Monooxygenase

CITE Title : A Carbonate-Forming Baeyer-Villiger Monooxygenase Personal Author(s) : Hu, Youcai;Dietrich, David;Xu, Wei;Patel, Ashay;Thuss, Justin A. J.;Wang, Jingjing;Yin, Wen-Bing;Qiao, Kangjian;Houk, Kendall N.;Vederas, John C.;Tang, Yi; Published Date : 7 2014;7-2014; Source : Nat Chem Biol. 10(7):552-554 URL : https://stacks.cdc.gov/view/cdc/27888 Hu, Youcai et al. (2014). A Carbonate-Forming Baeyer-Villiger Monooxygenase. 10(7). Hu, Youcai et al. "A Carbonate-Forming Baeyer-Villiger Monooxygenase" 10, no. 7 (2014) Hu, Youcai et al. "A Carbonate-Forming Baeyer-Villiger Monooxygenase" vol. 10, no. 7, 2014 Export RIS Citation Information.

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Hu, Youcai ;

Dietrich, David

7 2014 | Nat Chem Biol. 10(7):552-554

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Despite the remarkable versatility displayed by flavin-dependent monooxygenases (FMOs) in natural product biosynthesis, one notably missing activity i...