Journal
ORGANIC LETTERS
Volume 14, Issue 1, Pages 94-97Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol202883v
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Funding
- NIH-NIGMS [R01-GM096129]
- Alfred P. Sloan Foundation
- Amgen
- Boehringer Ingelheim
- Novartis Institutes for BioMedical Research
- NSF
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Our previous studies into visible-light-mediated aza-Henry reactions demonstrated that molecular oxygen played a vital role in catalyst turnover as well as the production of base to facilitate the nucleophilic addition of nitroalkanes. Herein, improved conditions for the generation of iminium Ions from tetrahydroisoquinolines that allow for versatile nucleophilic trapping are reported. The new conditions provide access to a diverse range of functionality under mild, anaerobic reaction conditions as well as mechanistic insights into the photoredox cycle.
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