Bisannulation of Benzamides and Cyclohexadienone-Tethered Allenes Triggered by Cp*Rh(III)-Catalyzed C-H Activation and Relay Ene Reaction.
| Author | |
|---|---|
| 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 
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| Journal | 
   :  
              Organic letters 
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| Date Published | 
   :  
              2018 
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| ISSN Number | 
   :  
              1523-7060 
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| DOI | 
   :  
              10.1021/acs.orglett.8b00083 
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| Short Title | 
   :  
              Org Lett 
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