Publications_zotero

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Total publications: 76


 

1.
Kumarasamy, E., Kandappa, S. K., Raghunathan, R., Jockusch, S. & Sivaguru, J. Realizing an Aza Paternò–Büchi Reaction. Angewandte Chemie International Edition 56, 7056–7061 (2017). Cite
1.
Kumagai, T., Shimizu, K., Kawamura, Y. & Mukai, T. Photochemistry of 3-aryl-2-isoxazoline 1 1 Organic Photochemistry 50. Part 49: K. Okada, K. Hisamitsu and T. Mukai, J. Chem. Soc. Chem. Comm. 941 (1980). Tetrahedron 37, 3365–3376 (1981). Cite
1.
Photochemistry UV/VIS spectroscopy, photochemical reactions and photosynthesis. (Nova Science Publishers, 2011). Cite
1.
Sakamoto, R., Inada, T., Sakurai, S. & Maruoka, K. [2 + 2] Photocycloadditions between the Carbon–Nitrogen Double Bonds of Imines and Carbon–Carbon Double Bonds. Org. Lett. 18, 6252–6255 (2016). Cite
1.
Sampedro, D. Computational Exploration of the Photocycloaddition of Imines to Alkenes. ChemPhysChem 7, 2456–2459 (2006). Cite
1.
Hyatt, J. A. & Swenton, J. S. Photochemical reactivity of 2,4-dimethyl-1,2,4-triazine-3,5-(2H)-dione (1,3-dimethyl-6-azauracil). J. Chem. Soc., Chem. Commun. 1144–1145 (1972) http://doi.org/10.1039/C39720001144. Cite
1.
Sampedro, D., Soldevilla, A., Campos, P. J., Ruiz, R. & Rodríguez, M. A. Regio- and Stereochemistry of [2 + 2] Photocycloadditions of Imines to Alkenes: A Computational and Experimental Study. J. Org. Chem. 73, 8331–8336 (2008). Cite
1.
Koch, T. H. & Howard, K. H. 2+2 Photocycloaddition to a carbon nitrogen double bond I. 3-ethoxyisoindolone. Tetrahedron Letters 13, 4035–4038 (1972). Cite
1.
Swenton, J. S. & Hyatt, J. A. Photosensitized cycloadditions to 1,3-dimethyl-6-azauracil and 1,3-dimethyl-6-azathymine. Imine linkage unusually reactive toward photocycloaddition. J. Am. Chem. Soc. 96, 4879–4885 (1974). Cite
1.
Koch, T. H. & Howard, K. H. 2+2 Photocycloaddition to a carbon nitrogen double bond I. 3-ethoxyisoindolone. Tetrahedron Letters 13, 4035–4038 (1972). Cite
1.
Howard, K. A. & Koch, T. H. Photochemical reactivity of keto imino ethers. V. (2 + 2) Photocycloaddition to the carbon-nitrogen double bond of 3-ethoxyisoindolone. J. Am. Chem. Soc. 97, 7288–7298 (1975). Cite
1.
Rodehorst, R. M. & Koch, T. H. Photochemical reactivity of keto imino ethers. VI. Type I rearrangement and (2 + 2) photocycloaddition to the carbon-nitrogen double bond of 2-oxazolin-4-ones. J. Am. Chem. Soc. 97, 7298–7304 (1975). Cite
1.
Tsuge, O., Tashiro, M. & Oe, K. Photochemical reaction of 2,5-diphenyl-1,3,4-oxadiazole with indene. Tetrahedron Letters 9, 3971–3974 (1968). Cite
1.
Tsuge, O., Oe, K. & Tashiro, M. Photochemistry of heterocyclic compounds—II: The photochemical reaction of 2,5-disubstituted 1,3,4-oxadiazoles with furan. Tetrahedron 29, 41–46 (1973). Cite
1.
Padwa, Albert. Photochemistry of the carbon-nitrogen double bond. Chem. Rev. 77, 37–68 (1977). Cite
1.
Pratt, A. C. The photochemistry of imines. Chem. Soc. Rev. 6, 63–81 (1977). Cite
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Tiefenthaler, H., Dörscheln, W., Göth, H. & Schmid, H. Photoisomerisierung von Pyrazolen und Indazolen zu Imidazolen bzw. Benzimidazolen und 2-Amino-benzonitrilen. Helvetica Chimica Acta 50, 2244–2258 (1967). Cite
1.
Lahmani, F. & Ivanoff, N. Photoisomerization of pyrazine and of its methyl derivatives. Tetrahedron Letters 8, 3913–3917 (1967). Cite
1.
Allison, C. G., Chambers, R. D., Cheburkov, Yu. A., MacBride, J. A. H. & Musgrave, W. K. R. The isomerisation of perfluoropyridazines to perfluoropyrimidines and to perfluoropyrazines. J. Chem. Soc. D 1200–1201 (1969) http://doi.org/10.1039/C29690001200. Cite
1.
Ohashi, M., Iio, A. & Yonezawa, T. Photoisomerization of phenylisothiazoles. J. Chem. Soc. D 1148–1148 (1970) http://doi.org/10.1039/C29700001148. Cite
1.
Beak, Peter. & Miesel, J. L. The photorearrangement of 2,3-dihydropyrazines. J. Am. Chem. Soc. 89, 2375–2384 (1967). Cite
1.
Kojima, M. & Maeda, M. Photorearrangements of 2,5- and 2,4-diphenylthiazole. J. Chem. Soc. D 386b–3387 (1970) http://doi.org/10.1039/C2970000386B. Cite
1.
Tiefenthaler, H., Dörscheln, W., Göth, H. & Schmid, H. Photoisomerisation von indazolen zu benzimidazolen. Tetrahedron Letters 5, 2999–3001 (1964). Cite
1.
Tiefenthaler, H., Dörscheln, W., Göth, H. & Schmid, H. Photoisomerisation von indazolen zu benzimidazolen. Tetrahedron Letters 5, 2999–3001 (1964). Cite
1.
Ullman, E. F. & Singh, B. Photochemical Transposition of Ring Atoms in Five-Membered Heterocycles. The Photorearrangement of 3,5-Diphenylisoxazole. J. Am. Chem. Soc. 88, 1844–1845 (1966). Cite
1.
Furey, R. L. & Kan, R. O. The photochemical hydrolysis of n-substituted imines. Tetrahedron 24, 3085–3093 (1968). Cite
1.
Toshima, N. & Hirai, H. Photochemical oxidation of imines. Tetrahedron Letters 11, 433–436 (1970). Cite
1.
Beckett, A. & Porter, G. Primary photochemical processes in aromatic molecules. Part 9.—Photochemistry of benzophenone in solution. Trans. Faraday Soc. 59, 2038–2050 (1963). Cite
1.
Singh, Balwant. & Ullman, E. F. Photochemical transposition of ring atoms in 3,5-diarylisoxazoles.  Unusual example of wavelength control in a photochemical reaction of azirines. J. Am. Chem. Soc. 89, 6911–6916 (1967). Cite
1.
Cerutti, P. & Schmid, H. Photoreaktionen von Methanol mit N-Heterocyclen 1. Mitteilung. Helvetica Chimica Acta 45, 1992–2004 (1962). Cite
1.
Cerutti, P. & Schmid, H. Photoreaktionen von Methanol mit N-Heterocyclen 2. Mitteilung. Helvetica Chimica Acta 47, 203–213 (1964). Cite
1.
Fischer, M. Photoreduktion von benzophenonimiden. Tetrahedron Letters 7, 5273–5277 (1966). Cite
1.
Padwa, A., Bergmark, W. & Pashayan, D. Mechanism of the photoreduction of N-Alkylbenzylidenimines. J. Am. Chem. Soc. 91, 2653–2660 (1969). Cite
1.
Padwa, A., Bergmark, W. & Pashayan, D. Photoreduction of benzaldehyde N-alkylimines. J. Am. Chem. Soc. 90, 4458–4459 (1968). Cite
1.
Reductions in organic synthesis: recent advances and practical applications. (American Chemical Society, 1996). Cite
1.
Huyser, E. S., Wang, R. H. S. & Short, W. T. Photochemical and peroxide induced reductions of benzophenone imine with secondary alcohols. J. Org. Chem. 33, 4323–4325 (1968). Cite
1.
Spagnuolo, C. J. Reductions in Organic Chemistry. Second Edition. ACS Monograph 188 By Milos Hudlicky. American Chemical Society, Washington, D.C. 1996. xxvi + 429 pp. 15.5 × 23.5 cm. ISBN 0-8412-3344-6. $109.95. J. Med. Chem. 41, 260–261 (1998). Cite
1.
Cannon, J. G. Comprehensive Organic Functional Group Transformations Edited by A. R. Katritzky, O. Meth-Cohn, and C. W. Rees. Pergamon Press (Elsevier Science Ltd.), Tarrytown, NY. 1995. 7 vols., 19.5 × 28 cm. vol. 1, xix + 1420 pp; vol. 2, xix + 1441 pp; vol. 3, xix + 941 pp; vol. 4, xix + 1352 pp; vol. 5, xix + 1442 pp; vol. 6, xix + 933 pp; vol. 7, xvii + 1251 pp. ISBN 0-08-042-322-1; 0-08-042-323-X; 0-08-042-324-8; 0-08-0442-325-6; 0-08-042-326-4; 0-08-042-704-9; 0-08-042-705-7. $4310 (set). J. Med. Chem. 40, 1940–1940 (1997). Cite
1.
Salvatore, R. N., Yoon, C. H. & Jung, K. W. Synthesis of secondary amines. Tetrahedron 57, 7785–7811 (2001). Cite
1.
Padwa, A., Bergmark, W. & Pashayan, D. Photoreduction of benzaldehyde N-alkylimines. J. Am. Chem. Soc. 90, 4458–4459 (1968). Cite
1.
Koch, T. H., Sluski, R. J. & Moseley, R. H. Photochemical reactivity of keto imino ethers.  IV.  Type I and type II reactions. J. Am. Chem. Soc. 95, 3957–3963 (1973). Cite
1.
Koch, T. H., Sluski, R. J. & Moseley, R. H. Photochemical reactivity of keto imino ethers.  IV.  Type I and type II reactions. J. Am. Chem. Soc. 95, 3957–3963 (1973). Cite
1.
Koch, T. H., Sluski, R. J. & Moseley, R. H. Photochemical reactivity of keto imino ethers.  IV.  Type I and type II reactions. J. Am. Chem. Soc. 95, 3957–3963 (1973). Cite
1.
Berbasova, T. et al. Light-Activated Reversible Imine Isomerization: Towards a Photochromic Protein Switch. Chembiochem 17, 407–414 (2016). Cite
1.
Padwa, A. & Albrecht, F. Concentration effects in the photochemical syn-anti isomerization of an oxime ether. J. Org. Chem. 39, 2361–2366 (1974). Cite
1.
Padwa, A. & Albrecht, F. Photochemical syn-anti isomerization about the carbon-nitrogen double bond. J. Am. Chem. Soc. 96, 4849–4857 (1974). Cite
1.
Padwa, A. & Albrecht, F. Excimer involvement in the photoisomerization of an oxime ether. Tetrahedron Letters 15, 1083–1086 (1974). Cite
1.
Hantzsch, A. Die stereochemisch-isomeren Oxime des p-Tolyl-Phenylketons. Berichte der deutschen chemischen Gesellschaft 23, 2325–2332 (1890). Cite
1.
Padwa, A. & Albrecht, F. Photoisomerization about the carbon-nitrogen double bond of an oxime ether. J. Am. Chem. Soc. 94, 1000–1002 (1972). Cite
1.
Padwa, A. & Albrecht, F. Photochemical syn-anti isomerization about the carbon-nitrogen double bond. J. Am. Chem. Soc. 96, 4849–4857 (1974). Cite

 

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