Dihydropyrones as dienophiles in the Diels-Alder reaction: Application to the synthesis of 1-oxadecalones

被引:42
|
作者
Chen, DQ [1 ]
Wang, JQ [1 ]
Totah, NI [1 ]
机构
[1] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 1999年 / 64卷 / 06期
关键词
D O I
10.1021/jo982488g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:1776 / 1777
页数:2
相关论文
共 50 条
  • [1] Dihydropyrones as dienophiles in the Diels-Alder reaction.
    Chen, DQ
    Totah, NI
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 213 : 173 - ORGN
  • [2] Synthesis of 1-oxadecalones via the Lewis acid catalyzed dihydropyrone Diels-Alder reaction
    Seth, PP
    Totah, NI
    JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (23): : 8750 - 8753
  • [3] THE DIELS-ALDER REACTION OF PYRIDAZINONES AS DIENOPHILES
    MATYUS, P
    FUJI, K
    TANAKA, K
    HETEROCYCLES, 1993, 36 (09) : 1975 - 1978
  • [4] Fluoropropenoates as dienophiles in the Diels-Alder reaction
    Patrick, Timothy B.
    Fianu, Cynthia
    Pak, Eric
    Zaksas, Kasey
    Neal, Bradley E.
    JOURNAL OF FLUORINE CHEMISTRY, 2006, 127 (07) : 861 - 864
  • [5] Diels-Alder Reaction with Hydrophilic Dienes and Dienophiles
    Shrinidhi, Annadka
    CHEMISTRYSELECT, 2016, 1 (12): : 3016 - 3021
  • [6] THE DIELS-ALDER REACTION ETHYLENIC AND ACETYLENIC DIENOPHILES
    HOLMES, HL
    ORGANIC REACTIONS, 1947, 4 : 60 - 173
  • [7] DIELS-ALDER REACTION OF FURAN WITH SOME DIENOPHILES
    EGGELTE, TA
    KONING, HD
    HUISMAN, HO
    TETRAHEDRON, 1973, 29 (16) : 2491 - 2493
  • [8] Masked Ketenes as Dienophiles in the Diels-Alder Reaction
    Mackay, Emily G.
    Newton, Christopher G.
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2016, 69 (12) : 1365 - 1374
  • [9] Diels-Alder reaction of heterocyclic imine dienophiles
    Hedberg, C
    Pinho, P
    Roth, P
    Andersson, PG
    JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (09): : 2810 - 2812
  • [10] Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis
    Nawrat, Christopher C.
    Moody, Christopher J.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (08) : 2056 - 2077