Recent Advances in 1,3-Dipolar Cycloaddition Reactions on Solid Supports

ChemInform ◽  
2005 ◽  
Vol 36 (32) ◽  
Author(s):  
Kirsi Harju ◽  
Jari Yli-Kauhaluoma
ChemInform ◽  
2005 ◽  
Vol 36 (32) ◽  
Author(s):  
Avijit Banerji ◽  
Debasish Bandyopadhyay

2018 ◽  
Vol 16 (44) ◽  
pp. 8446-8461 ◽  
Author(s):  
Silvia Roscales ◽  
Joaquín Plumet

In this review recent advances in the metal-catalyzed 1,3-dipolar cycloaddition reactions of nitrile oxides are highlighted, covering references from the period 2000 until August 2018.


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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