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Volume 8, Issue 2 (Suppl)

Chem Sci J 2017

ISSN: 2150-3494 CSJ, an open access journal

Euro Chemistry 2017

May 11-13, 2017

May 11-13, 2017 Barcelona, Spain

4

th

European Chemistry Congress

Palladium catalyzed domino heck/aryne carbopalladation/c-h functionalization: Synthesis of heterocycle-

fused 9,10-dihydrophenanthrenes

Tuanli Yao

Shaanxi University of Science and Technology, China

A

rynes generated from the corresponding o-(trimethylsilyl)aryl triflates have emerged as powerful synthons in organic synthesis.

Aryne annulation reactions with intramolecular C-H functionalization can be a powerful method for the synthesis of polycyclic

compounds. We developed a novel palladium-catalyzed domino Heck/aryne carbopalladation/C-H functionalization reaction using

in situ generated arynes, in which three new C-C bonds and a carbon quaternary center are formed. This methodology affords

moderate to excellent yields of heterocycle-fused 9,10-dihydrophenanthrenes.

Biography

Tuanli Yao has completed his PhD from Iowa State University and postdoctoral studies from University of California, Berkeley. He worked as Senior Scientist

at Deciphera Pharmaceuticals and Associate Researcher at University of Kansas before beginning his career in academy. Currently, he is professor at Shaanxi

University of Science & Technology. His research interests include aryne chemistry, electrophilic cyclization and palladium catalysis. He has published more than

30 papers in reputed journals.

yaotuanli@sust.edu.cn

Tuanli Yao, Chem Sci J 2017, 8:2(Suppl)

http://dx.doi.org/10.4172/2150-3494-C1-008