ChemInform Abstract: 1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins with Chloramine-T. Part 2.

ChemInform ◽  
2001 ◽  
Vol 32 (4) ◽  
pp. no-no
Author(s):  
V. Padmavathi ◽  
R. P. Sumathi ◽  
K. Venugopal Reddy ◽  
A. Somasekhar Reddy ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins with Chloramine-T --- Part-II

2000 ◽  
Vol 30 (22) ◽  
pp. 4007-4016 ◽  
Author(s):  
V. Padmavathi ◽  
R. P. Sumathi ◽  
K. Venugopal Reddy ◽  
A. Somasekhar Reddy ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Bis Olefins in the Presence of Chloramine-T

2003 ◽  
Vol 178 (1) ◽  
pp. 171-177 ◽  
Author(s):  
V. Padmavathi ◽  
K. Venugopal Reddy ◽  
A. Padmaja ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

1,3-Dipolar Cycloaddition of Dipolar Reagents to Bischalcones in the Presence of Chloramine-T.

ChemInform ◽  
2005 ◽  
Vol 36 (5) ◽  
Author(s):  
V. Padmavathi ◽  
K. Venugopal Reddy ◽  
M. Rajagopala Sarma ◽  
R. P. Sumathi ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

ChemInform Abstract: 1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins in the Presence of Chloramine-T (CAT).

ChemInform ◽  
2010 ◽  
Vol 31 (7) ◽  
pp. no-no
Author(s):  
V. Padmavathi ◽  
R. P. Sumathi ◽  
N. Chandrasekhar Babu ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

scholarly journals 3-Benzoylisoxazolines by 1,3-Dipolar Cycloaddition: Chloramine-T-Catalyzed Condensation of α-Nitroketones with Dipolarophiles

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3491
Author(s):  
Xinhui Pan ◽  
Xiaobing Xin ◽  
Ying Mao ◽  
Xin Li ◽  
Yanan Zhao ◽  
...  
Keyword(s):  
Low Cost ◽  
Dipolar Cycloaddition ◽  
Chloramine T

In this study, 3-benzoylisoxazolines were synthesized by reacting alkenes with various α-nitroketones using chloramine-T as the base. The scope of α-nitroketones and alkenes is extensive, including different alkenes and alkynes to form various isoxazolines and isoxazoles. The use of chloramine-T, as the low-cost, easily handled, moderate base for 1,3-dipolar cycloaddition is attractive.

scholarly journals 1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins in the Presence of Chloramine-T (CAT)

1999 ◽  
Vol 23 (10) ◽  
pp. 610-611
Author(s):  
V. Padmavathi ◽  
R. P. Sumathi ◽  
N. Chandrasekhar Babu ◽  
D. Bhaskar Reddy
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T

2-Pyrazolines and 2-isoxazolines are prepared by the reaction of araldehyde hydrazones and araldoximes with bifunctional olefins in the presence of chloramine-T, which also functions as a reagent for aromatization of the former.

1,3-Dipolar Cycloaddition of Dipolar Reagents to Bifunctional Olefins in the Presence of Chloramine-T (CAT)

1999 ◽  
pp. 610-611 ◽  
Author(s):  
V. Padmavathi ◽  
R. P. Sumathi ◽  
N. Chandrasekhar Babu ◽  
D. Bhaskar
Keyword(s):  
Dipolar Cycloaddition ◽  
Chloramine T
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