INTRAMOLECULAR ALKYLATION OF PHENOLS .5. A REGIOSPECIFIC ANIONIC RING-CLOSURE OF PHENOLS VIA QUINONE METHIDES

被引:22
作者
MURPHY, WS
WATTANASIN, S
机构
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1980年 / 07期
关键词
D O I
10.1039/p19800001567
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:1567 / 1577
页数:11
相关论文
共 50 条
  • [1] REGIOSPECIFIC ALKYLATION OF PHENOLS - ORTHO OR PARA TO ALPHA-COUPLING IN CYCLIZATION OF BIS-PHENOLS VIA QUINONE METHIDES
    MURPHY, WS
    WATTANASIN, S
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1979, (18) : 788 - 789
  • [2] DEHYDROGENATION OF STEROIDAL PHENOLS VIA QUINONE METHIDES
    BROWN, W
    FINDLAY, JWA
    TURNER, AB
    CHEMICAL COMMUNICATIONS, 1968, (01) : 10 - &
  • [3] New construction of ortho ring-alkylated phenols via generation and reaction of assorted quinone methides.
    Pettus, T
    Van De Water, R
    Magdziak, D
    Chau, J
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U206 - U206
  • [4] New construction of ortho ring-alkylated phenols via generation and reaction of assorted o-quinone methides
    Van de Water, RW
    Magdziak, DJ
    Chau, JN
    Pettus, TRR
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (27) : 6502 - 6503
  • [5] CHEMISTRY OF REACTIVE LIGNIN INTERMEDIATES .5. RATES OF REACTIONS OF QUINONE METHIDES WITH WATER, ALCOHOLS, PHENOLS, AND CARBOXYLIC-ACIDS
    LEARY, G
    MILLER, IJ
    THOMAS, W
    WOOLHOUSE, AD
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1977, (13): : 1737 - 1739
  • [6] A mild anionic method for generating o-quinone methides:: Facile preparations of ortho-functionalized phenols
    Jones, RM
    Van de Water, RW
    Lindsey, CC
    Hoarau, C
    Ung, T
    Pettus, TRR
    JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (10) : 3435 - 3441
  • [7] STUDIES ON INTRAMOLECULAR ALKYLATION .5. INTRAMOLECULAR ALKYLATION OF AROMATIC RING IN TETRAHYDRONAPHTHYL DIAZOMETHYL KETONES
    BEAMES, DJ
    KLOSE, TR
    MANDER, LN
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1974, 27 (06) : 1269 - 1275
  • [8] Mild anionic method for generating ortho-quinone methides:: Facile preperations of ortho-functionalized phenols.
    Jones, R
    Van de Water, RW
    Lindsey, C
    Hoarau, C
    Ung, T
    Pettus, TRR
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 221 : U207 - U207
  • [9] Straightforward Synthesis of Bifunctional Phosphorus Phenols via Phosphination of In Situ Generated o-Quinone Methides
    Chen, Zhangpei
    Shi, Qinglong
    Wang, Gongshu
    Chen, Siwen
    Hu, Jianshe
    MOLECULES, 2018, 23 (06):
  • [10] O-(ALPHA-BENZOTRIAZOLYLALKYL)PHENOLS - NOVEL PRECURSORS FOR THE PREPARATION OF ORTHO-SUBSTITUTED PHENOLS VIA INTERMEDIATE O-QUINONE METHIDES
    KATRITZKY, AR
    ZHANG, ZX
    LAN, XF
    LANG, HY
    JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (07) : 1900 - 1903