Transition metal-catalyzed chlorine transfer cyclizations of carbon-centered glycine radicals; A novel synthetic route to cyclic α-amino acids

Tetrahedron ◽  
1994 ◽  
Vol 50 (6) ◽  
pp. 1907-1918 ◽  
Author(s):  
Jan H. Udding ◽  
C. (Kees) J.M. Tuijp ◽  
Henk Hiemstra ◽  
W. Nico Speckamp
2002 ◽  
Vol 74 (1) ◽  
pp. 159-166 ◽  
Author(s):  
Iwao Ojima

Recent development in the transition metal-catalyzed cyclization reactions for organic syntheses in the author's laboratories is summarized, which includes (i) novel silylcarbocyclizations (SiCaCs) and carbonylative carbotricyclizations, (ii) intramolecular silylformylations and desymmerization of siloxydiynes by sequential double silylformylation, (iii) efficient total synthesis of (+)-prosopinine, (iv) enantioselective desymmetrization of aminodienes, and (iv) new and efficient routes to 1-azabicyclo[x.y.0]alkane amino acids. All these processes are catalyzed by Rh or Rh­Co complexes, and useful for rapid and efficient construction of a variety of heterocyclic and carbocyclic compounds. Mechanisms of these new carbocyclization and cyclohydrocarbonylation reactions are also discussed.


RSC Advances ◽  
2016 ◽  
Vol 6 (99) ◽  
pp. 96762-96767 ◽  
Author(s):  
Krishna K. Sharma ◽  
Meenakshi Mandloi ◽  
Neha Rai ◽  
Rahul Jain

A transition metal-catalyzed, environmentally benign, rapid and cost-effective method for the N-(hetero)arylation of zwitterionic amino acids in water is reported.


Author(s):  
Jin-Wei Yuan ◽  
Chenxu Mou ◽  
Yang Zhang ◽  
Wenyu Hu ◽  
Liangru Yang ◽  
...  

A practical synthetic route to construct a variety of 3-benzyl spiro[4,5]trienones was developed via transition-metal Cu/Ag-catalyzed oxidative ipso-annulation of activated alkynes with unactivated toluenes using TBPB as an oxidant under...


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