Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin

被引:49
|
作者
Parkan, Kamil [1 ]
Pohl, Radek [2 ]
Kotora, Martin [3 ]
机构
[1] Inst Chem Technol, Dept Chem Nat Cpds, CR-16628 Prague 6, Czech Republic
[2] Acad Sci Czech Republ, Inst Organ Chem & Biochem, Vvi, CR-16610 Prague 6, Czech Republic
[3] Charles Univ Prague, Fac Sci, Dept Organ Chem, Prague 12843 2, Czech Republic
关键词
CC coupling; glycosides; natural products; protecting groups; synthetic methods; METAL-MODIFIED SUGARS; REDUCTIVE AROMATIZATION; ORGANOBORON DERIVATIVES; PAPULACANDIN-C; SPIROKETAL; ELECTROPHILES; EPOXIDATION; STRATEGIES; GLYCOSIDES; NUCLEUS;
D O I
10.1002/chem.201304304
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A convenient synthetic pathway enabling D-glucal and D-galactal pinacol boronates to be prepared in good isolated yields was achieved. Both pinacol boronates were tested in a series of cross-coupling reactions under Suzuki-Miyaura cross-coupling conditions to obtain the corresponding aryl, heteroaryl, and alkenyl derivatives in high isolated yields. This methodology was applied to the formal synthesis of the glucopyranoside moiety of papulacandinD and the first total synthesis of bergenin.
引用
收藏
页码:4414 / 4419
页数:6
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