1246523-57-8Relevant articles and documents
Concise syntheses of dictyodendrins A and F by a sequential C-H functionalization strategy
Yamaguchi, Atsushi D.,Chepiga, Kathryn M.,Yamaguchi, Junichiro,Itami, Kenichiro,Davies, Huw M. L.
, p. 644 - 647 (2015)
Syntheses of dictyodendrins A and F have been achieved using a sequential C-H functionalization strategy. The N-alkylpyrrole core is fully functionalized by means of a rhodium(I)-catalyzed C-H arylation at the C3-position, a rhodium(II)-catalyzed double C-H insertion at the C2- and C5-positions, and a Suzuki-Miyaura cross-coupling reaction at the C4-position. The syntheses of dictyodendrins A and F were completed by formal 6π-electrocyclization to generate the pyrrolo[2,3-c]carbazole core of the natural products.
Total synthesis of dictyodendrin A and B
Okano, Kentaro,Fujiwara, Hideto,Noji, Toshiharu,Fukuyama, Tohru,Tokuyama, Hidetoshi
supporting information; experimental part, p. 5925 - 5929 (2010/10/03)
(Figure Presented) In-do-line of fire: A highly efficient total synthesis of the title compounds features a novel benzyne-mediated one-pot indoline formation/cross-coupling sequence for the construction of a highly substituted key indoline intermediate. The peripheral substituents were then introduced onto the intermediate in a modular fashion to complete the total syntheses of dictyodendrin A and B.