| Literature DB >> 30067041 |
Jie S Zhu1, Niklas Kraemer1, Marina E Shatskikh1, Clarabella J Li1, Jung-Ho Son1, Makhluf J Haddadin2, Dean J Tantillo1, Mark J Kurth1.
Abstract
A concise, one-step route to indazolones from primary alkyl amines and o-nitrobenzyl alcohols is reported. The key step in this readily scalable indazolone forming process involves base-mediated in situ o-nitrobenzyl alcohol → o-nitrosobenzaldehyde conversion. Although this functional group interconversion is known to be useful for 2 H-indazole synthesis, its reactivity was modulated for indazolone formation.Entities:
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Year: 2018 PMID: 30067041 PMCID: PMC6451655 DOI: 10.1021/acs.orglett.8b01655
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005