Search Results - Naga Siva Rao, J.

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  1. 1
    (4'-Acet-yloxy-1,3,1'-trioxo-1,3,4,4a,4b,5,6,7,9,9a-deca-hydro-spiro-[indene-2,9'-pyrano[4,3-a]pyrrolizin]-3'-yl)methyl acetate

    (4'-Acet-yloxy-1,3,1'-trioxo-1,3,4,4a,4b,5,6,7,9,9a-deca-hydro-spiro-[indene-2,9'-pyrano[4,3-a]pyrrolizin]-3'-yl)methyl acetate by Latha, N, Naga Siva Rao, J, Raghunathan, R, Divya, G, Lakshmi, S

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  2. 2
    A facile synthesis of glyco 3-nitrochromane hybrid pyrrolidinyl spiro heterocycles via [3+2] cycloaddition of azomethine ylides

    A facile synthesis of glyco 3-nitrochromane hybrid pyrrolidinyl spiro heterocycles via [3+2] cycloaddition of azomethine ylides by Naga Siva Rao, J., Raghunathan, R.

    Published in Tetrahedron letters
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  3. 3
    An expedient diastereoselective synthesis of pyrrolidinyl spirooxindoles fused to sugar lactone via [3+2] cycloaddition of azomethine ylides

    An expedient diastereoselective synthesis of pyrrolidinyl spirooxindoles fused to sugar lactone via [3+2] cycloaddition of azomethine ylides by Naga Siva Rao, J., Raghunathan, R.

    Published in Tetrahedron letters
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  4. 4
    A tactical 1,3-dipolar cycloaddition approach for the synthesis of carbohydrate derived polycyclic spiro heterocycles

    A tactical 1,3-dipolar cycloaddition approach for the synthesis of carbohydrate derived polycyclic spiro heterocycles by Rao, J. Naga Siva, Raghunathan, R.

    Published in Tetrahedron letters
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  5. 5
    An expedient synthesis of pyrrolidinyl spirooxindole grafted 3-nitrochromanes through 1,3-dipolar cycloaddition reaction of azomethine ylides

    An expedient synthesis of pyrrolidinyl spirooxindole grafted 3-nitrochromanes through 1,3-dipolar cycloaddition reaction of azomethine ylides by Naga Siva Rao, J., Raghunathan, R.

    Published in Tetrahedron letters
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  6. 6
    One-pot sequential azide–alkyne/intramolecular azomethine ylide 1,3-dipolar cycloaddition strategy for the synthesis of carbohydrate grafted macrocycles

    One-pot sequential azide–alkyne/intramolecular azomethine ylide 1,3-dipolar cycloaddition strategy for the synthesis of carbohydrate grafted macrocycles by Rao, J. Naga Siva, Raghunathan, R.

    Published in Tetrahedron letters
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  7. 7
    6a-Nitro-6-(2,2,7,7-tetramethyltetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4′,5′-d]pyran-5-yl)-6a,6b,7,8,9,11a-hexahydro-6H-spiro[chromeno[3,4-a]pyrrolizine-11,11′-indeno[1,2-b]quinoxaline]

    6a-Nitro-6-(2,2,7,7-tetramethyltetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4′,5′-d]pyran-5-yl)-6a,6b,7,8,9,11a-hexahydro-6H-spiro[chromeno[3,4-a]pyrrolizine-11,11′-indeno[1,2-b]quinoxalin... by T. Anuradha, J. Naga Siva Rao, P. R. Seshadri, R. Raghunathan

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  8. 8
    6a-Nitro-6-(2,2,7,7-tetra-methyl-tetra-hydro-3aH-bis-[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl)-6a,6b,7,8,9,11a-hexa-hydro-6H-spiro-[chromeno[3,4-a]pyrrolizine-11,11'-indeno-[1,2-b]quinoxaline]

    6a-Nitro-6-(2,2,7,7-tetra-methyl-tetra-hydro-3aH-bis-[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl)-6a,6b,7,8,9,11a-hexa-hydro-6H-spiro-[chromeno[3,4-a]pyrrolizine-11,11'-indeno-[1,2-b]qui... by Anuradha, T, Naga Siva Rao, J, Seshadri, P R, Raghunathan, R

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  9. 9
    (1S,1′S,2′R,4a'S,9a'S,9b'R)-1′-Acetyloxy-2,4′-dioxo-2′,4′,4a',7′,8′,9′,9a',9b'-octahydro-1′H,2H-spiro[acenaphthylene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate

    (1S,1′S,2′R,4a'S,9a'S,9b'R)-1′-Acetyloxy-2,4′-dioxo-2′,4′,4a',7′,8′,9′,9a',9b'-octahydro-1′H,2H-spiro[acenaphthylene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate... by S. Santhiya, J. Naga Siva Rao, R. Raghunathan, N. Latha, S. Lakshmi

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  10. 10
    6a-Nitro-6-(2,2,7,7-tetramethyltetrahydro-3a H -bis[1,3]dioxolo[4,5- b :4′,5′- d ]pyran-5-yl)-6a,6b,7,8,9,11a-hexahydro-6 H -spiro[chromeno[3,4- a ]pyrrolizine-11,11′-indeno[1,2- b ]quinoxaline]

    6a-Nitro-6-(2,2,7,7-tetramethyltetrahydro-3a H -bis[1,3]dioxolo[4,5- b :4′,5′- d ]pyran-5-yl)-6a,6b,7,8,9,11a-hexahydro-6 H -spiro[chromeno[3,4- a ]pyrrolizine-11,11′-indeno[1,2- b... by Anuradha, T., Naga Siva Rao, J., Seshadri, P. R., Raghunathan, R.

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  11. 11
    (1 S ,1′ S ,2′ R ,4a' S ,9a' S ,9b' R )-1′-Acetyloxy-2,4′-dioxo-2′,4′,4a',7′,8′,9′,9a',9b'-octahydro-1′ H ,2 H -spiro[acenaphthylene-1,5′-pyrano[4,3- a ]pyrrolizin]-2′-ylmethyl acetate

    (1 S ,1′ S ,2′ R ,4a' S ,9a' S ,9b' R )-1′-Acetyloxy-2,4′-dioxo-2′,4′,4a',7′,8′,9′,9a',9b'-octahydro-1′ H ,2 H -spiro[acenaphthylene-1,5′-pyrano[4,3- a ]pyrrolizin]-2′-ylmethyl ace... by Santhiya, S., Naga Siva Rao, J., Raghunathan, R., Latha, N., Lakshmi, S.

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  12. 12
    (1S,1'S,2'R,4a'S,9a'S,9b'R)-1'-Acet-yloxy-2,4'-dioxo-2',4',4a',7',8',9',9a',9b'-octa-hydro-1'H,2H-spiro-[ace-naphthyl-ene-1,5'-pyrano[4,3-a]pyrrolizin]-2'-ylmethyl acetate

    (1S,1'S,2'R,4a'S,9a'S,9b'R)-1'-Acet-yloxy-2,4'-dioxo-2',4',4a',7',8',9',9a',9b'-octa-hydro-1'H,2H-spiro-[ace-naphthyl-ene-1,5'-pyrano[4,3-a]pyrrolizin]-2'-ylmethyl acetate by Santhiya, S, Naga Siva Rao, J, Raghunathan, R, Latha, N, Lakshmi, S

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  13. 13
    (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate

    (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate... by Santhiya, S., Naga Siva Rao, J., Raghunathan, R., Latha, N., Lakshmi, S.

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