Journal
ORGANIC LETTERS
Volume 18, Issue 13, Pages 3130-3133Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01334
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Funding
- NSFC [21372268, 21372266]
- Fundamental Research Funds for the Central Universities [106112016CDJZR228806]
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The reaction of a domino aryne precursor with sulfonamides efficiently afforded both 1,3-diaminobenzenes and trisubstituted 1,3-diaminobenzenes by simply varying the reaction conditions. Mechanistic study supports the sequential formation of two transient aryne intermediates involved in-the reaction.
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