Pictet-Spengler reactions of Nb-hydroxytryptamines and their application to the synthesis of eudistomins

被引：0
|
作者：
Hino, T [1 ]
Nakagawa, M [1 ]
机构：
[1] Chiba Univ, Fac Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
来源：
HETEROCYCLES | 1998年 / 49卷
关键词：
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Methods for preparing Nb-hydroxytryptamines, their Pictet-Spengler reactions with various aldehydes via nitrones, and their asymmetric inductions are reviewed. Syntheses of oxathiazepine-containing eudistomins and related natural products which incorporate these reactions are also reviewed.
引用
收藏
页码：499 / 530
页数：32
相关论文
共 50 条
  • [21] THE PICTET-SPENGLER SYNTHESIS OF TETRAHYDROISOQUINOLINES AND RELATED COMPOUNDS
    WHALEY, WM
    GOVINDACHARI, TR
    ORGANIC REACTIONS, 1951, 6 : 151 - 190
  • [22] Application of hexamethylenetetramine in a Pictet-Spengler type reaction for synthesis of isoquinoline derivatives
    Ivanov, I
    Venkov, A
    HETEROCYCLES, 2001, 55 (08) : 1569 - 1572
  • [23] Regioselectivity of Pictet-Spengler cyclization: synthesis of halotetrahydroisoquinolines
    Cho, SD
    Song, SY
    Hur, EJ
    Chen, M
    Joo, WH
    Falck, JR
    Yoon, YJ
    Shin, DS
    TETRAHEDRON LETTERS, 2001, 42 (36) : 6251 - 6253
  • [24] STEREOSELECTIVE PICTET-SPENGLER REACTIONS - APPLICATION TO THE SYNTHESIS OF OPTICALLY-ACTIVE TETRAHYDRO BETA-CARBOLINES
    REDDY, MS
    COOK, JM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 207 : 312 - ORGN
  • [25] Synthesis of aza-quaternary centers via Pictet-Spengler reactions of ketonitrones
    Lynch-Colameta, Tessa
    Greta, Sarah
    Snyder, Scott A.
    CHEMICAL SCIENCE, 2021, 12 (17) : 6181 - 6187
  • [26] Ionic liquid in organic synthesis: The Pictet-Spengler reaction
    Wang, Huey-Min
    Hou, Rei-Sheu
    Huang, Hsin-Yu
    Chen, Ling-Ching
    HETEROCYCLES, 2006, 68 (08) : 1651 - 1658
  • [27] ASYMMETRIC PICTET-SPENGLER SYNTHESIS OF TETRAHYDROISOQUINOLINES - AN ENANTIOSELECTIVE SYNTHESIS OF (-)-LAUDANOSINE
    COMINS, DL
    BADAWI, MM
    TETRAHEDRON LETTERS, 1991, 32 (26) : 2995 - 2996
  • [28] Microwave assisted Pictet-Spengler and Bischler-Napieralski reactions
    Pal, B
    Jaisankar, P
    Giri, VS
    SYNTHETIC COMMUNICATIONS, 2003, 33 (13) : 2339 - 2348
  • [29] Asymmetric synthesis of tetrahydroisoquinolines by enzymatic Pictet-Spengler reaction
    Nishihachijo, Masakatsu
    Hirai, Yoshinori
    Kawano, Shigeru
    Nishiyama, Akira
    Minami, Hiromichi
    Katayama, Takane
    Yasohara, Yoshihiko
    Sato, Fumihiko
    Kumagai, Hidehiko
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2014, 78 (04) : 701 - 707
  • [30] NON-REGIOSELECTIVITY OF THE PICTET-SPENGLER TETRAHYDROISOQUINOLINE SYNTHESIS
    BATES, HA
    VERTINO, PM
    GARELICK, JS
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1984, 188 (AUG): : 198 - ORGN
12345