Journal
ORGANIC LETTERS
Volume 18, Issue 7, Pages 1666-1669Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00534
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Funding
- National Natural Science Foundation of China [21272190]
- NFFTBS [J1310024]
- PCSIRT in University
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A novel method for the preparation of 5,6-dihydropyrazolo [5,1-a]isoquinoline via indium(III)-promoted halocyclizations of N-propargylic sulfonylhydrazones has been developed. The pyrazole and 3,4-dihydroisoquinoline moieties were synchronously formed via a cascade cyclization reaction using easily assembled open-chain compounds. The pyrazole and 3,4-dihydroisoquinoline moieties were formed via a cascade cyclization reaction using easily assembled open chain compounds.
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