Journal
CHEMICAL COMMUNICATIONS
Volume 48, Issue 62, Pages 7696-7698Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc33269h
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Funding
- Shanghai Municipal Committee of Science and Technology [11JC1402600]
- National Basic Research Program of China (973) [2009CB825300]
- National Natural Science Foundation of China [21072206, 20472096, 20872162, 20672127, 20732008, 21121062]
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A facile synthetic method of functionalized pyrrolo[1,2-a]indoles has been developed via a thermally-induced ring-opening and cyclization reaction from aniline-tethered alkylidenecyclopropanes with aldehydes.
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