Low Energy Collision-Induced Dissociation of Azepine Pictet–Spengler Adducts of Nω-Methylserotonin
Author:
Affiliation:
1. Department of Pharmaceutical Sciences UIC/NIH Center for Botanical Dietary Supplements Research College of Pharmacy, University of Illinois at Chicago 833 S. Wood St., Chicago, Illinois 60612-7231, United States
Funder
Office of Dietary Supplements
National Center for Complementary and Integrative Health
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
https://pubs.acs.org/doi/pdf/10.1021/jasms.2c00247
Reference23 articles.
1. The Pictet-Spengler Reaction in Nature and in Organic Chemistry
2. The Pictet-Spengler condensation: a new direction for an old reaction
3. The Chemistry of Indoles. CVII. A Novel Synthesis of 3,4,5,6-Tetrahydro-7-hydroxy-1H-azepino[5,4,3-cd]indoles and a New Finding on Pictet-Spengler Reaction.
4. Formation of 3,4,5,6-Tetrahydro-7-hydroxy-6-methyl-1H-azepino[5,4,3-cd]indole in the Reaction of Serotonin with Acetaldehyde in Water in the Presence of Either L-Amino Acid, Nicotine or Fluoride
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