The [1,3] O-to-C rearrangement: opportunities for stereoselective synthesis

被引:68
|
作者
Nasveschuk, Christopher G. [1 ]
Rovis, Tomislav [1 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
关键词
D O I
10.1039/b714881j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The relay of stereochemistry of a breaking C-O bond into a forming C-C bond is well-known in the context of [3, 3] sigmatropic shifts; however, this useful strategy is less well-known in other types of molecular rearrangements. Though the first successful example of a [1, 3] O-to-C rearrangement was reported more than 100 years ago, this class of reactions has received less attention than its [3, 3] counterpart. This perspective analyzes the various methods used for the activation and [1, 3] rearrangement of vinyl ethers with an emphasis on mechanism and applications to stereoselective synthesis. We also highlight our own contributions to this area.
引用
收藏
页码:240 / 254
页数:15
相关论文
共 50 条
  • [1] Catalytic [1,3]O-to-C Rearrangement: Rapid Access to Bridged Bicyclic Systems
    Zhang, Jiantao
    Liao, Zhehui
    Chen, Lianfen
    Jiang, Huanfeng
    Zhu, Shifa
    CHEMISTRY-A EUROPEAN JOURNAL, 2018, 24 (27) : 6927 - 6931
  • [2] Palladium-Catalyzed [1,3]-O-to-C Rearrangement of Pyrans toward Functionalized Cyclohexanones
    Brioche, Julien C. R.
    Barker, Thomas A.
    Whatrup, David J.
    Barker, Michael D.
    Harrity, Joseph P. A.
    ORGANIC LETTERS, 2010, 12 (21) : 4832 - 4835
  • [3] Asymmetric dearomatization of benzyl 1-naphthyl ethers via [1,3] O-to-C rearrangement
    Zeng, Hongkun
    Wen, Gang
    Lin, Lili
    Feng, Xiaoming
    CHEMICAL COMMUNICATIONS, 2024, 60 (58) : 7507 - 7510
  • [4] Chiral Fe(ii) complex catalyzed enantioselective [1,3] O-to-C rearrangement of alkyl vinyl ethers and synthesis of chromanols and beyond
    Wang, Lifeng
    Zhou, Pengfei
    Lin, Qianchi
    Dong, Shunxi
    Liu, Xiaohua
    Feng, Xiaoming
    CHEMICAL SCIENCE, 2020, 11 (37) : 10101 - 10106
  • [5] Enantioselective Construction of C4-Quaternary Quinolinones via Copper(II)-Catalyzed Asymmetric [1,3] O-to-C Rearrangement
    Xiong, Zongli
    Xu, Fuxing
    Zhou, Yuqiao
    Zhang, Rong
    Zhang, Yulong
    Chen, Yushuang
    Yao, Weijun
    Wang, Zhen
    ORGANIC LETTERS, 2023, 25 (46) : 8302 - 8307
  • [6] Enantioselective [1,3] O-to-C rearrangement: dearomatization of alkyl 2-allyloxy/benzyloxy-1/3-naphthoates catalyzed by a chiral π-Cu(II) complex
    Yao, Lu
    Ishihara, Kazuaki
    CHEMICAL SCIENCE, 2019, 10 (08) : 2259 - 2263
  • [7] Gold(I) catalyzed [1,3] O → C rearrangement of benzylvinyl ethers
    Kona, Chandrababu Naidu
    Patil, Mahesh N.
    Ramana, Chepuri V.
    ORGANIC CHEMISTRY FRONTIERS, 2016, 3 (04): : 453 - 456
  • [8] Gold(I)-catalysed [1,3] O→C rearrangement of allenyl ethers
    Kona, Chandrababu Naidu
    Ramana, Chepuri V.
    CHEMICAL COMMUNICATIONS, 2014, 50 (17) : 2152 - 2154
  • [9] Stereoselective synthesis of medium lactams enabled by metal-free hydroalkoxylation/stereospecific [1,3]-rearrangement
    Zhou, Bo
    Zhang, Ying-Qi
    Zhang, Kairui
    Yang, Ming-Yang
    Chen, Yang-Bo
    Li, You
    Peng, Qian
    Zhu, Shou-Fei
    Zhou, Qi-Lin
    Ye, Long-Wu
    NATURE COMMUNICATIONS, 2019, 10 (1)
  • [10] Stereoselective synthesis of medium lactams enabled by metal-free hydroalkoxylation/stereospecific [1,3]-rearrangement
    Bo Zhou
    Ying-Qi Zhang
    Kairui Zhang
    Ming-Yang Yang
    Yang-Bo Chen
    You Li
    Qian Peng
    Shou-Fei Zhu
    Qi-Lin Zhou
    Long-Wu Ye
    Nature Communications, 10