1,3,4,5-tetrahydroazepin-2-ones by dearomatising anionic cyclisation of N-allyl-1-naphthamides

被引:26
作者
Ahmed, A
Clayden, J
Rowley, M
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
[2] Merck Sharp & Dohme Ltd, Neurosci Res Ctr, Harlow CM20 2QR, Essex, England
关键词
amide; cyclization; lithium; azepin; dearomatisation;
D O I
10.1055/s-1999-2977
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
On treatment with t-BuLi and DMPU, 1-naphthamides bearing N-allyl or N-prenyl substituents cyclise to give a mixture of products from which seven-membered lactams can be isolated in up to 73% yield - the first example of an organolithium-C=C cyclisation leading to a seven-membered ring.
引用
收藏
页码:1954 / 1956
页数:3
相关论文
共 50 条
  • [41] Domino reactions of 1-(2-alkoxyaryl)-3-akylprop-2-yn-1-ones with sodium sulfide leading to thiochromen-4-one derivatives
    Yang, Xiaobo
    Li, Shangfu
    Liu, Hongxia
    Jiang, Yuyang
    Fu, Hua
    RSC ADVANCES, 2012, 2 (16): : 6549 - 6554
  • [42] Bromenium-Catalysed Tandem Ring Opening/Cyclisation of Vinylcyclopropanes and Vinylcyclobutanes: A Metal-Free [3+2+1]/[4+2+1] Cascade for the Synthesis of Chiral Amidines and Computational Investigation
    Ganesh, Venkataraman
    Sureshkumar, Devarajulu
    Chanda, Debasree
    Chandrasekaran, Srinivasan
    CHEMISTRY-A EUROPEAN JOURNAL, 2012, 18 (39) : 12498 - 12511
  • [43] Preparation of Halogen-Containing 4H-Pyrido[e][1,3]oxazin-4-ones and Their Transformation into 2-Hydroxypyridinyl-Substituted 1,2,4-Oxadiazoles and 1,2,4-Triazoles
    Le Falher, Laetitia
    Ben Ayad, Omar
    Ziyaret, Ozge
    Botuha, Candice
    Thorimbert, Serge
    Slowinski, Franck
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2015, 2015 (17) : 3830 - 3840
  • [44] Gold(I)-catalyzed intramolecular [4+2] cycloaddition of ortho-(N-tethered 1,6-diynyl)benzaldehydes to 3,4-dihydrobenzo[flisoquinolin-1(2H)-ones
    Zhong, Jiankai
    Hu, Rui
    Sang, Jingjing
    Rao, Weidong
    TETRAHEDRON LETTERS, 2020, 61 (31)
  • [45] [2-(2-Nitrophenyl)oxiran-1-yl](aryl(methyl))ketones in the synthesis of 3-hydroxyquinolin-4(1H)-ones and 2-arylquinolines
    Mamedov, V. A.
    Mamedova, V. L.
    Khikmatova, G. Z.
    Mahrous, E. M.
    Korshin, D. E.
    Syakaev, V. V.
    Fayzullin, R. R.
    Mironova, E. V.
    Latypov, Sh. K.
    Sinyashin, O. G.
    RUSSIAN CHEMICAL BULLETIN, 2019, 68 (05) : 1020 - 1024
  • [46] 4-Substituted 5-nitroisoquinolin-1-ones from intramolecular Pd-catalysed reaction of N-(2-alkenyl)-2-halo-3-nitrobenzamides
    Dhami, Archana
    Mahon, Mary F.
    Lloyd, Matthew D.
    Threadgill, Michael D.
    TETRAHEDRON, 2009, 65 (24) : 4751 - 4765
  • [47] Preparation of a Select Tautomer of Various Unsymmetrical 1,3,5-Pentanetriones, (1Z,4Z)-1-(Aryl)-1,5-dihydroxy-5-phenylpenta-1,4-dien-3-ones, a 4H-1-benzothiopyran-4-one, and a 2-(2-oxoyl)quinolin-4(1H)-one
    Mabe, Phillip J. Chase
    Knick, Shabree L.
    Shuler, William G.
    Carlisle, Sarah S.
    Smith, Ellyn A.
    Puciaty, Andrew J.
    McFadden, Thomas M. C.
    Potter, Chandra
    Metz, Clyde R.
    Beam, Charles F.
    Pennington, William T.
    VanDerveer, Donald G.
    McMillan, Colin D.
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2015, 54 (29) : 7207 - 7211
  • [48] Synthesis of 4,4-disubstituted-4H-benzo[d][1,3]oxathiin-2-ones, a new class of compounds
    Kamila, S
    Khan, O
    Zhang, HM
    Biehl, ER
    SYNTHETIC COMMUNICATIONS, 2006, 36 (10) : 1419 - 1429
  • [49] Iodine promoted dual oxidative C(sp3)-H amination of 2-methyl-3-arylquinazolin-4(3H)-ones: a facile route to 1,4-diarylimidazo[1,5-a]quinazolin-5(4H)-ones
    Donthiboina, Kavitha
    Namballa, Hari Krishna
    Shaik, Siddiq Pasha
    Nanubolu, Jagadeesh Babu
    Shankaraiah, Nagula
    Kamal, Ahmed
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2018, 16 (10) : 1720 - 1727
  • [50] Design, synthesis and cytotoxicity evaluation of novel (E)-3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-1-(pyridin-3-yl)prop-2-en-1-ones as anticancer agents
    Alam, Raquib
    Alam, Md. Aftab
    Panda, Amulya K.
    Uddin, Rahis
    HETEROCYCLIC COMMUNICATIONS, 2016, 22 (04) : 221 - 225