Catalytic Asymmetric [4+2] Cycloaddition of in Situ Generated o-Quinone Methide Imines with o-Hydroxystyrenes: Diastereo- and Enantioselective Construction of Tetrahydroquinoline Frameworks

2018 ◽  
Vol 83 (2) ◽  
pp. 614-623 ◽  
Author(s):  
Lin-Zhi Li ◽  
Cong-Shuai Wang ◽  
Wei-Feng Guo ◽  
Guang-Jian Mei ◽  
Feng Shi
2014 ◽  
Vol 17 (2) ◽  
pp. 176-179 ◽  
Author(s):  
Linqing Wang ◽  
Dongxu Yang ◽  
Fengxia Han ◽  
Dan Li ◽  
Depeng Zhao ◽  
...  
Keyword(s):  

2019 ◽  
Vol 84 (12) ◽  
pp. 7829-7839 ◽  
Author(s):  
Jin-Rong Wang ◽  
Xiao-Li Jiang ◽  
Qing-Qing Hang ◽  
Shu Zhang ◽  
Guang-Jian Mei ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (35) ◽  
pp. no-no
Author(s):  
Lorenzo Caruana ◽  
Martina Mondatori ◽  
Vasco Corti ◽  
Sara Morales ◽  
Andrea Mazzanti ◽  
...  

ChemInform ◽  
1988 ◽  
Vol 19 (1) ◽  
Author(s):  
Y. GAO ◽  
R. M. HANSON ◽  
J. M. KLUNDER ◽  
S. Y. KO ◽  
H. MASAMUNE ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (98) ◽  
pp. 80212-80215 ◽  
Author(s):  
N. J. Willis ◽  
C. D. Bray
Keyword(s):  

A method for the generation/in situhetero-Diels–Alder cycloaddition of a trisubstitutedortho-quinone methide (o-QM) is described.


2020 ◽  
Vol 18 (28) ◽  
pp. 5388-5399 ◽  
Author(s):  
Shu-Fang Wu ◽  
Man-Su Tu ◽  
Qing-Qing Hang ◽  
Shu Zhang ◽  
Haixia Ding ◽  
...  

The title reaction has been established in the presence of chiral phosphoric acid, affording chiral chroman derivatives bearing an indole moiety in high yields and with moderate to good stereoselectivities.


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