Chiral (.eta.6-arene)chromium complexes in organic synthesis: stereoselective synthesis of chiral (arene)chromium complexes possessing amine and hydroxy groups and their application to asymmetric reactions

1993 ◽  
Vol 58 (5) ◽  
pp. 1238-1244 ◽  
Author(s):  
Motokazu Uemura ◽  
Ryuta Miyake ◽  
Kazuo Nakayama ◽  
Motoo Shiro ◽  
Yuji Hayashi
ChemInform ◽  
2010 ◽  
Vol 22 (43) ◽  
pp. no-no
Author(s):  
M. UEMURA ◽  
H. NISHIMURA ◽  
T. MINAMI ◽  
Y. HAYASHI

Synlett ◽  
2020 ◽  
Vol 31 (18) ◽  
pp. 1741-1746
Author(s):  
Shenqqing Zhu ◽  
Lingling Chu ◽  
Fang Wang

Catalytic, stereoselective synthesis of skipped dienes is an important topic in organic synthesis. Summarized here are the transition-metal-catalyzed stereoselective approaches and a new, photoinduced stereodivergent strategy reported by our group recently. Our strategy utilizes a synergistic photoredox/nickel protocol to enable the cross-electrophile coupling of allylic carbonates and vinyl triflates to construct 1,4-dienes, the stereoselectivity of which was tuned by the triplet energy (E T) photocatalysts employed, offering a convenient and stereodivergent solution to (E)- and (Z)-1,4-dienes from one set of substrates.


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