Bisannulation of Benzamides and Cyclohexadienone-Tethered Allenes Triggered by Cp*Rh(III)-Catalyzed C-H Activation and Relay Ene Reaction.
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| Abstract | :  The diastereoselective bisannulation of N-(pivaloyloxy)benzamides and cyclohexadienone-tethered allenes was accomplished through Cp*Rh(III)-catalyzed C-H activation and relay ene reaction, providing a 3-isoquinolonyl cis-hydrobenzofuran framework with high yields and diastereoselectivities. This reaction tolerates a wide range of functional groups, enabling further conversions to tricyclic and bridged-ring structures. Moreover, the dearomatization modification of phenol-contained bioactive molecule is also elaborated. | 
| Year of Publication | :  2018 | 
| Journal | :  Organic letters | 
| Date Published | :  2018 | 
| ISSN Number | :  1523-7060 | 
| DOI | :  10.1021/acs.orglett.8b00083 | 
| Short Title | :  Org Lett | 
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