Rapid Access to Tricyclic Systems: Highly Endoselective Diels—Alder Reaction of Cycloalkenones with Cyclic Dienes under Microwave Irradiation.

ChemInform ◽  
2004 ◽  
Vol 35 (17) ◽  
Author(s):  
M. Karthikeyan ◽  
R. Kamakshi ◽  
V. Sridar ◽  
B. S. R. Reddy
1985 ◽  
Vol 16 (28) ◽  
Author(s):  
M. G. VELIEV ◽  
M. M. GUSEINOV ◽  
L. A. YANOVSKAYA ◽  
K. YA. BURSTEIN

2017 ◽  
Vol 53 (10) ◽  
pp. 1657-1659 ◽  
Author(s):  
Jun Li ◽  
Hai-Yan Tao ◽  
Chun-Jiang Wang

A highly efficient enantioselective nitroso Diels–Alder reaction of 6-methyl-2-nitroso pyridine with various 1,3-dienes was successfully developed using a copper(i)/(S)–TF-BiphamPhos complex as the catalyst. For most of the cyclic dienes, the cycloadducts were obtained in high yields with excellent regio-, and stereoselectivities. Acyclic 2-silyloxy-1,3-diene also worked well in the reaction.


Tetrahedron ◽  
1985 ◽  
Vol 41 (4) ◽  
pp. 749-761 ◽  
Author(s):  
M.G. Veliev ◽  
M.M. Guseinov ◽  
L.A. Yanovskaya ◽  
K.Ya. Burstein

1986 ◽  
Vol 108 (25) ◽  
pp. 8021-8027 ◽  
Author(s):  
Glenn C. Calhoun ◽  
Gary B. Schuster

Tetrahedron ◽  
1986 ◽  
Vol 42 (6) ◽  
pp. 1769-1777 ◽  
Author(s):  
Stephen F. Nelsen ◽  
Silas C. Blackstock ◽  
Timothy B. Frigo

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