Synthesis and Application of [3.3.0]Furofuranone in Total Synthesis

被引:13
|
作者
Peng, Xiao-Shui [1 ,2 ,3 ,4 ]
Ylagan, Ridge Michael P. [1 ,2 ]
Siu, Yuk Ming [1 ,2 ]
Wong, Henry N. C. [1 ,2 ,3 ,4 ]
机构
[1] Chinese Univ Hong Kong, Ctr Novel Funct Mol, State Key Lab Synthet Chem, Dept Chem, Sha Tin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Inst Mol Funct Mat, Sha Tin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Shenzhen Res Inst, Shenzhen Ctr Novel Funct Mol, Shenzhen 518507, Peoples R China
[4] Chinese Univ Hong Kong, Shenzhen Municipal Key Lab Chem Synth Med Organ M, Shenzhen 518507, Peoples R China
基金
中国国家自然科学基金;
关键词
domino reactions; furofuranones; natural products; synthesis; total synthesis; DIELS-ALDER ADDUCTS; DIASTEREOSELECTIVE TOTAL-SYNTHESIS; STEREOSELECTIVE TOTAL-SYNTHESIS; MODIFIED WESSELY OXIDATION; BAEYER-VILLIGER OXIDATION; SPONGE PLAKORTIS-SIMPLEX; ACID-DIRECTED REACTIONS; 1ST TOTAL-SYNTHESIS; AB RING-SYSTEM; ENANTIOSELECTIVE SYNTHESIS;
D O I
10.1002/asia.201500288
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and application of [3.3.0]furofuranone species has received considerable attention from the scientific community. During the last twenty years, there has been a remarkable increase in publications focusing on their relevant method development as well as applications to natural product synthesis. This tutorial review discusses instructive examples to give a special emphasis on the development of new synthetic approaches and important applications to the total synthesis of natural products.
引用
收藏
页码:2070 / 2083
页数:14
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