Metal‐Catalyzed Quinoid Carbene ( QC ) Transfer Reactions

2021 ◽  
pp. 269-297
Author(s):  
Hai‐Xu Wang ◽  
Vanessa K.‐Y. Lo ◽  
Chi‐Ming Che
1993 ◽  
Vol 12 (11) ◽  
pp. 4289-4290 ◽  
Author(s):  
Guilaine Veneziani ◽  
Regis Reau ◽  
Guy Bertrand

2018 ◽  
Vol 9 (3) ◽  
pp. 546-559 ◽  
Author(s):  
Tao Jia ◽  
Peng Cao ◽  
Jian Liao

To date, enantiomerically enriched molecules containing gem(1,1)-diaryl containing tertiary or quaternary stereogenic centers have been readily accessed by transition metal-catalyzed enantioselective or stereoconvergent aryl transfer reactions.


2018 ◽  
Vol 26 (19) ◽  
pp. 5270-5273 ◽  
Author(s):  
Juliet M. Alderson ◽  
Joshua R. Corbin ◽  
Jennifer M. Schomaker

Synlett ◽  
2019 ◽  
Vol 30 (12) ◽  
pp. 1377-1383 ◽  
Author(s):  
Janakiram Vaitla ◽  
Annette Bayer ◽  
Kathrin H. Hopmann

Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed reactions. The stability and reactivity of sulfoxonium ylides depend on the substitution of the ylide carbon. The reactivity of vinyl-substituted sulfoxonium ylides is different and offers several advantages over known stabilized sulfoxonium ylides in the case of carbenoid transfer reactions. Herein, we provide an overview of early efforts in this area, with particular emphasis on our own recent development of sulfoxonium ylide-derived vinyl carbenoid transformations for N-Heterocycles.1 Introduction2 Classification of Sulfoxonium Ylides3 Synthesis of Vinyl Sulfoxonium Ylides4 [3+2] Annulation of Vinyl Sulfoxonium Ylides5 [4+1] Annulation of Vinyl Sulfoxonium Ylides6 Conclusion


2006 ◽  
Vol 35 (3) ◽  
pp. 237 ◽  
Author(s):  
Joseph S. M. Samec ◽  
Jan-E. Bäckvall ◽  
Pher G. Andersson ◽  
Peter Brandt

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