Biomimetic Phosphate-Catalyzed Pictet–Spengler Reaction for the Synthesis of 1,1′-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids
Author:
Affiliation:
1. Department of Chemistry, University College London, Christopher Ingold Building, 20 Gordon Street, London WC1H 0AJ, U.K.
2. Department of Biochemical Engineering, University College London, London WC1E 6BT, U.K.
Funder
Engineering and Physical Sciences Research Council
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00527
Reference37 articles.
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3. Synthesis and evaluation of furoxan-based nitric oxide-releasing derivatives of tetrahydroisoquinoline as anticancer and multidrug resistance reversal agents
4. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics
5. Bronchodilator and anti-inflammatory activities of glaucine:In vitrostudies in human airway smooth muscle and polymorphonuclear leukocytes
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2. Interfacing Whole Cell Biocatalysis with a Biocompatible Pictet‐Spengler Reaction for One‐Pot Syntheses of Tetrahydroisoquinolines and Tryptolines**;ChemBioChem;2023-10-25
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4. Convenient synthesis of 8‐aryl‐6‐aryl‐1,2,3,4‐tetrahydroisoquinoline‐5,7‐dicarbonitriles via a cascade Michael/cyclization reaction;Journal of the Chinese Chemical Society;2022-03-30
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