Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Krishan Singal"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 45:361-364
1,3-Dipolar cycloaddition of nitrile oxides generated in situ in the presence of variously substituted N-arylmaleimides and N-benzylmaleimide provides new pyrrolo[3,4-d]izoxazoline-4,6-diones in good yields. The whole procedure could be performed in
Autor:
Kewal Krishan Singal, Jaswinder Kaur
Publikováno v:
Synthetic Communications. 31:2809-2815
[2 + 2] Cycloaddition reactions of benzyne generated in situ with various substituted azomethines have been carried out leading to the synthesis of 1,2-diarylbenzazetidenes in good yields with a high degree of regioselectivity.
Publikováno v:
Synthetic Communications. 29:911-915
Through the cycloaddition of N-(α-cyano-α-aryl)-methylanilines (II) on to N-sulphinylanilines (III) are synthesized 2,3,5-triaryl-4-imino-2H, 3H, 5H-[1.2.5]thiadiazoIidin-l-oxides (TV) in aood vields.
Autor:
Kewal Krishan Singal
Publikováno v:
Synthetic Communications. 26:3571-3577
New substituted isoxazolidine derivatives have been synthesized through regiospecific and stereospecific 1,3-dipolar cycloadditions of C-(2-nitro)-styryl-N-phenyl nitrone with reactive dipolarophiles in excellent yields and effects of substituents ha
Publikováno v:
Synthetic Communications. 23:107-114
1,4-Diaryl-1-aza-1, 3-butadienes (I) undergo a stereospecific 1,4-cycloaddition reaction with aryl sulphonyl nitrosites (II) generated ‘in situ’ by the reaction of aryl sulphinic acid and ethyl nitrite to yield six-membered cycloadducts character
Publikováno v:
ChemInform. 24
Autor:
Kewal Krishan Singal
Publikováno v:
ChemInform. 27
New substituted isoxazolidine derivatives have been synthesized through regiospecific and stereospecific 1,3-dipolar cycloadditions of C-(2-nitro)-styryl-N-phenyl nitrone with reactive dipolarophiles in excellent yields and effects of substituents ha
Publikováno v:
ChemInform. 30
Publikováno v:
ChemInform. 30
Autor:
Kewal Krishan Singal, Jaswinder Kaur
Publikováno v:
ChemInform. 33
[2 + 2] Cycloaddition reactions of benzyne generated in situ with various substituted azomethines have been carried out leading to the synthesis of 1,2-diarylbenzazetidenes in good yields with a high degree of regioselectivity.