Regioselectivity of 1,3-dipolar cycloaddition reactions of C-acetyl-N-arylnitrilimines with acrylic acid derivatives and .alpha.,.beta.-unsaturated ketones

1989 ◽  
Vol 34 (2) ◽  
pp. 259-262 ◽  
Author(s):  
Ahmad S. Shawali ◽  
Saleh T. Ezmirly ◽  
Hamdi M. Hassaneen
1973 ◽  
Vol 4 (34) ◽  
pp. no-no
Author(s):  
GIORGIO BIANCHI ◽  
CARLO DE MICHELI ◽  
REMO GANDOLFI ◽  
PAOLO GRUENANGER ◽  
PAOLO VITA FINZI ◽  
...  

2013 ◽  
Vol 17 (18) ◽  
pp. 1929-1956 ◽  
Author(s):  
Natarajan Arumugam ◽  
Raju Kumar ◽  
Abdulrahman Almansour ◽  
Subbu Perumal

2002 ◽  
Vol 67 (3) ◽  
pp. 353-364 ◽  
Author(s):  
Petr Melša ◽  
Ctibor Mazal

Diastereoselectivity of 1,3-dipolar cycloaddition reactions of benzyl azide, diazomethane, a nitrile oxide and a nitrile imine to α-methylidene-γ-lactone dipolarophile was effectively controlled by a bulky γ-substituent, 4-methyl-2,6,7-trioxabicyclo[2.2.2]octan-1-yl in γ-position of the dipolarophile. The dipoles added from the less hindered face of the double bond with an excellent selectivity. Enantiomerically pure dipolarophile was prepared from the easily available (S)-5-oxotetrahydrohydrofuran-2-carboxylic acid.


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