TY - JOUR
T1 - Synthetic studies on goniodomin A
T2 - Convergent assembly of the C15-C36 segment via palladium-catalyzed organostannane-thioester coupling
AU - Saito, Tomoyuki
AU - Fuwa, Haruhiko
AU - Sasaki, Makoto
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research (A) (No. 21241050 ) from the Japan Society for the Promotion of Science (JSPS) and the Tohoku University Global COE program ‘International Center of Research & Education for Molecular Complex Chemistry’. T.S. is grateful for a SUNBOR Scholarship.
Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2011/1/14
Y1 - 2011/1/14
N2 - A stereocontrolled convergent synthesis of the C15-C36 segment of goniodomin A, a potent anti-angiogenic marine polyether macrolide, has been achieved using Stille-type cross-coupling reaction of a vinylstannane and a thioester as a key segment assembly process.
AB - A stereocontrolled convergent synthesis of the C15-C36 segment of goniodomin A, a potent anti-angiogenic marine polyether macrolide, has been achieved using Stille-type cross-coupling reaction of a vinylstannane and a thioester as a key segment assembly process.
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U2 - 10.1016/j.tet.2010.11.017
DO - 10.1016/j.tet.2010.11.017
M3 - Article
AN - SCOPUS:78650175131
VL - 67
SP - 429
EP - 445
JO - Tetrahedron
JF - Tetrahedron
SN - 0040-4020
IS - 2
ER -
