ol6b02665_si_005.cif (10.31 kB)

Stereospecific Synthesis of Tetrahydronaphtho[2,3‑b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization

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posted on 22.09.2016, 19:55 by Yu Peng, Jian Xiao, Xiao-Bo Xu, Shu-Ming Duan, Li Ren, Yong-Liang Shao, Ya-Wen Wang
A Ni-mediated cascade to a stereoselective synthesis of trans-tetrahydronaphtho­[2,3-b]­furans is efficiently achieved for the first time. The mild reductive system can be easily generated from inexpensive and air-stable materials and shows a broad positional tolerance of substituents that were previously difficult or impossible to access by other methods. Facile syntheses toward new analogues of therapeutic agents (iso)­deoxypodophyllotoxin are also reported. In addition, the inherent substrate control is disclosed for the observed unique stereoselectivities during cyclizations.

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