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- Tryptophol and derivatives: natural occurrence and applications to the synthesis of bioactive compounds. Alessandro Palmieri, Marino Petrini
, Nat. Prod. Rep.
, 2019
, 36
, 490
- Catalyst-free cyclization of anthranils and cyclic amines: one-step synthesis of rutaecarpine. Jian Li, Zheng-Bing Wang, Yue Xu, Xue-Chen Lu, Shang-Rong Zhu, Li Liu
, Chem. Commun.
, 2019
, 55
, 12072
- Molecularly imprinted solid phase extraction in an efficient analytical protocol for indole-3-methanol determination in artificial gastric juice. Dorota Klejn, Piotr Luliński, Dorota Maciejewska
, RSC Adv.
, 2016
, 6
, 108801
- Transcriptional control of the quorum sensing response in yeast. Arthur Wuster, M. Madan Babu
, Mol. BioSyst.
, 2009
, 6
, 134
- Water enables the tunable electrochemical synthesis of heterocyclic 3a- or 5a-bromoindolines. Ying-Ai Wu, Rui-An Wang, Shu-Yun Jiang, Tai-Bai Jiang, Jun-Rong Song, Jun Shi, Wei Wu, Wei-Dong Pan, Hai Ren
, Green Chem.
, 2022
, 24
, 6720
- An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives. Jun Xu, Rongbiao Tong
, Green Chem.
, 2017
, 19
, 2952
- Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast. Monika Bhardwaj, Shifali Chib, Loveleena Kaur, Amit Kumar, Bhabatosh Chaudhuri, Fayaz Malik, Ram A. Vishwakarma, Saurabh Saran, Debaraj Mukherjee
, RSC Med. Chem.
, 2020
, 11
, 142
- Insights into the regioselectivity and diastereoselectivity of the Nazarov cyclization of 3-alkenyl-2-indolylmethanol with tryptophol. Qi Cheng, Wenxin Yan, Tian Li, Yinchun Jiao, Zilong Tang
, Org. Chem. Front.
, 2023
, 10
, 1721
- Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis. Guang-Jian Mei, Wai Lean Koay, Chuan Xiang Alvin Tan, Yixin Lu
, Chem. Soc. Rev.
, 2021
, 50
, 5985
- Electrochemical synthesis of 3a-bromofuranoindolines and 3a-bromopyrroloindolines mediated by MgBr2. Ju Wu, Hussein Abou-Hamdan, Régis Guillot, Cyrille Kouklovsky, Guillaume Vincent
, Chem. Commun.
, 2020
, 56
, 1713