| Literature DB >> 29431446 |
Jie S Zhu1, Matthew R Duong1, Andrew P Teuthorn1, Julia Y Lu1, Jung-Ho Son1, Makhluf J Haddadin2, Mark J Kurth1.
Abstract
Reaction options, alkoxide vs hydroxide vs amine addition to the key intermediate (o-nitrosoimine) generated in the Davis-Beirut reaction of an o-nitrobenzylamine substrate, are reported to explain the nucleophilic addition selectivity of this one-pot indazole-forming process. The hydroxide addition/deprotection pathway as well as the fate of the resulting o-nitrosobenzaldehyde were both uncovered with several o-nitrobenzylamine substrates, and design elements required for an efficient double Davis-Beirut reaction, inspired by new mechanistic insights, were defined.Entities:
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Year: 2018 PMID: 29431446 PMCID: PMC6485925 DOI: 10.1021/acs.orglett.8b00036
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005