EFFECTIVE RING FORMATIONS AND NATURAL PRODUCT SYNTHESES

被引：13
|
作者：
FUKUMOTO, K
机构：
[1] Faculty of Pharmaceutical Sciences, Tohoku University
来源：
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN | 1994年 / 52卷 / 01期
关键词：
INTRAMOLECULAR DIELS-ALDER REACTION; INTRAMOLECULAR DOUBLE MICHAEL REACTION; TANDEM MICHAEL-ALDOL REACTION; TANDEM MICHAEL-CLAISEN REACTION; DOUBLE MICHAEL-ALDOL REACTION; TOTAL SYNTHESIS OF TERPENES; TOTAL SYNTHESIS OF STEROIDS; TOTAL SYNTHESIS OF ALKALOIDS;
D O I：
10.5059/yukigoseikyokaishi.52.2
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Simple and effective synthetic methods of polycylic ring systems in intramolecular reactions are presented. The first example is Diels-Alder reaction, which has been applied to total synthesis of steroids and terpenes. The intramolecular double Michael reaction is the second case, whose mechanism and application to natural product synthesis are also discussed. In addition, some related reactions of the latter are described.
引用
收藏
页码：2 / 18
页数：17
相关论文
共 50 条
  • [41] Syntheses of Bioactive Natural Products and Natural-Product-Like Compounds Based on Their Key Structural Units
    Zhang, Hongbin
    SYNLETT, 2014, 25 (14) : 1953 - 1970
  • [42] Progress in the Construction of Cyclooctanoid Systems: New Approaches and Applications to Natural Product Syntheses
    Mehta, Goverdhan
    Singh, Vishwakarma
    Chemical Reviews, 99 (03): : 881 - 930
  • [43] Highly effective total synthesis of benzofuran natural product egonol
    Choi, Da Hye
    Hwang, Jung Woon
    Lee, Hyun Suck
    Yang, Deok Mo
    Jun, Jong-Gab
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2008, 29 (08) : 1594 - 1596
  • [44] Evidence for limited diversity of ring size in monocyclic natural product macrocycles
    Sawwan, Nahed
    Farina, Nicola S.
    Frank, Aaron T.
    Wauchope, Orrette R.
    Qi, Mo
    Brzostowska, Edyta M.
    Haberfield, Paul
    Greer, Alexander
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U3463 - U3464
  • [45] Tandem ring-closing/cross metathesis in natural product synthesis
    Quinn, Kevin J.
    Smith, Austin G.
    Ortolani, John B.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 231
  • [46] LINEAMENTS AND RING FORMATIONS IN POLAND.
    Bazinski, J.
    Daniel-Danielska, B.
    Graniczny, M.
    Wilczinski, M.
    Soviet Journal of Remote Sensing (English translation of Issledovanie Zemmli iz Kosmosa), 1985, 2 (05): : 741 - 744
  • [47] A photochemical flow reactor for large scale syntheses of aglain and rocaglate natural product analogues
    Yueh, Han
    Gao, Qiwen
    Porco, John A., Jr.
    Beeler, Aaron B.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2017, 25 (23) : 6197 - 6202
  • [48] Vic-tricarbonyl compounds in natural product synthesis: Studies in total syntheses of preussochromones
    Koert, Ulrich
    Kerste, Eric
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [49] ORGANIC-PHOTOCHEMISTRY .15. APPLICATIONS OF PHOTOCYCLOADDITION REACTIONS IN NATURAL PRODUCT SYNTHESES
    DILLING, WL
    PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1977, 25 (06) : 605 - 621
  • [50] Formations, bihomomorphisms and natural transformations
    Ensor, A
    BULLETIN OF THE AUSTRALIAN MATHEMATICAL SOCIETY, 2000, 61 (02) : 217 - 239
12345