Peng-cheng Qian

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Name:
Organization: Wenzhou University
Department: College of Chemistry and Materials Engineering
Title:
Co-reporter:Bo-Lun Hu, Sha-Sha Pi, Peng-Cheng Qian, Jin-Heng Li, and Xing-Guo Zhang
The Journal of Organic Chemistry 2013 Volume 78(Issue 3) pp:1300-1305
Publication Date(Web):January 10, 2013
DOI:10.1021/jo302634n
A palladium-catalyzed, iodine-mediated electrophilic annulation between 2-(1-alkynyl)biphenyl and disulfide has been developed. With the combination of PdCl2 and I2, a variety of 2-(1-alkynyl)biphenyls underwent electrophilic annulations with various disulfides successfully to afford the corresponding 9-sulfenyl phenanthrenes in moderate to excellent yields.
6-Oxa-9-azaspiro[4.5]decane
6-methyl-3-phenyl-Imidazo[1,2-a]pyridine
3-(4-methylphenyl)-Imidazo[1,2-a]pyridine
3-(3-methylphenyl)-Imidazo[1,2-a]pyridine
7-methyl-3-phenyl-Imidazo[1,2-a]pyridine
2-Propyn-1-one, 1-(2,4-dimethoxyphenyl)-3-phenyl-
Thiophene, 2-(2-methylphenyl)-5-phenyl-
THIOPHENE, 2-(3-METHYLPHENYL)-5-PHENYL-
2-Propyn-1-one, 3-phenyl-1-[4-(trifluoromethyl)phenyl]-
2-Propyn-1-one, 1-[1,1'-biphenyl]-4-yl-3-phenyl-