A trans-vinylogous ester anion equivalent and its application to the synthesis of (+)-brefeldin A
暂无分享,去创建一个
Seung‐Yong Seo | Y. Suh | R. Jeon | Jae-Kyung Jung | O. Park
[1] C. Nájera,et al. Acylvinyl and vinylogous synthons. , 2000, Chemical reviews.
[2] K. Ohkura,et al. Elucidation of strict structural requirements of brefeldin A as an inducer of differentiation and apoptosis. , 2000, Bioorganic & medicinal chemistry.
[3] C. Mioskowski,et al. Enantioconvergent Formal Synthesis of Brefeldin A via Sakai-Catalyzed Cyclization , 1999 .
[4] B. Suh,et al. A FORMAL SYNTHESIS OF (+)-BREFELDIN A , 1998 .
[5] Y. Suh,et al. The highly diastereoselective palladium-catalyzed cyclizations. stereoselective syntheses of cis and trans-disubstituted hydroxycyclopentanes , 1997 .
[6] E. Grabowski,et al. A new general method for preparation of N-methoxy-N-methylamides. Application in direct conversion of an ester to a ketone , 1995 .
[7] A. Meyers,et al. (E)-1-Bromo-3,3-diethoxy-1-propene (diethyl acetal of 3-bromoacrolein). A versatile synthon for the synthesis of furans, butenolides, and (Z)-allyl alcohols , 1985 .
[8] E. Corey,et al. A new general synthetic route to bridged carboxylic ortho esters , 1984 .
[9] T. Katsuki,et al. A rapid esterification by means of mixed anhydride and its application to large-ring lactonization. , 1979 .
[10] D. Watt,et al. 1-Vinyl-4-methyl-2,6,7-trioxabicyclo[2.2.2]octanes: Unsaturated homoenolate anion equivalents , 1987 .