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
相关论文
共 50 条
  • [1] Total Synthesis of (+)-Rubriflordilactone A
    Goh, Shermin S.
    Chaubet, Guilhem
    Gockel, Birgit
    Cordonnier, Marie-Caroline A.
    Baars, Hannah
    Phillips, Andrew W.
    Anderson, Edward A.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (43) : 12618 - 12621
  • [2] Organocatalytic Enantiospecific Total Synthesis of Butenolides
    Madhavachary, Rudrakshula
    Mallik, Rosy
    Ramachary, Dhevalapally B.
    MOLECULES, 2021, 26 (14):
  • [3] Total Synthesis of Schilancitrilactones B and C
    Wang, Liang
    Wang, Hengtao
    Li, Yihang
    Tang, Pingping
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (19) : 5732 - 5735
  • [4] Total Synthesis of (+)-Cladospolide A
    Prasad, Kavirayani R.
    Revu, Omkar
    SYNTHESIS-STUTTGART, 2012, 44 (14): : 2243 - 2248
  • [5] Total Synthesis of (-)-Salinosporamide A
    Kaiya, Yuji
    Hasegawa, Jun-ichi
    Momose, Takayuki
    Sato, Takaaki
    Chida, Noritaka
    CHEMISTRY-AN ASIAN JOURNAL, 2011, 6 (01) : 209 - 219
  • [6] The Total Synthesis of Hyperforin
    Ting, Chi P.
    Maimone, Thomas J.
    SYNLETT, 2016, 27 (10) : 1443 - 1449
  • [7] Total Synthesis of Astellatol
    Zhao, Nan
    Yin, Shuqiang
    Xie, Shengling
    Yan, Hao
    Ren, Pan
    Chen, Gui
    Chen, Fang
    Xu, Jing
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (13) : 3386 - 3390
  • [8] Total Synthesis of Liangshanone
    Huang, Hong-Xiu
    Mi, Fen
    Li, Chunxin
    He, Huan
    Wang, Feng-Peng
    Liu, Xiao-Yu
    Qin, Yong
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (52) : 23609 - 23614
  • [9] Total Synthesis of (±)-Alstoscholarisine A
    Bihelovic, Filip
    Ferjancic, Zorana
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (07) : 2569 - 2572
  • [10] Total Synthesis of (-)-NakadomarinA
    Clark, J. Stephen
    Xu, Chao
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (13) : 4332 - 4335