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Turro

Turro N J 1978 Modern Moiecuiar Photochemistry Uen o Park, CA Benjamin-Cummings)... [Pg.1083]

Turro N J, Buchachenko A L and Tarasov V F 1995 How spin stereochemistry severely complicates the formation of a carbon-carbon bond between two reactive radicals in a supercage Acc. Chem. Res. 28 69-80... [Pg.1618]

Turro N J and Cherry W R 1978 Photoreaction in detergent soiutions. Enhancement of regioseiectivity resuiting from the reduced dimensionaiity of substrates sequestered in a miceiie J. Am. Chem. Soc. 100 7431-2... [Pg.2606]

The majority of preparative methods which have been used for obtaining cyclopropane derivatives involve carbene addition to an olefmic bond, if acetylenes are used in the reaction, cyclopropenes are obtained. Heteroatom-substituted or vinyl cydopropanes come from alkenyl bromides or enol acetates (A. de Meijere, 1979 E. J. Corey, 1975 B E. Wenkert, 1970 A). The carbenes needed for cyclopropane syntheses can be obtained in situ by a-elimination of hydrogen halides with strong bases (R. Kdstcr, 1971 E.J. Corey, 1975 B), by copper catalyzed decomposition of diazo compounds (E. Wenkert, 1970 A S.D. Burke, 1979 N.J. Turro, 1966), or by reductive elimination of iodine from gem-diiodides (J. Nishimura, 1969 D. Wen-disch, 1971 J.M. Denis, 1972 H.E. Simmons, 1973 C. Girard, 1974),... [Pg.74]

If a bromomethyl- or vinyl-substituted cyclopropane carbon atom bears a hydroxy group, the homoallyiic rearrangement leads preferentially to cyclobutanone derivatives (J. Sa-laun, 1974). Addition of amines to cydopropanone (N. J. Turro, 1966) yields S-lactams after successive treatment with tert-butyl hypochlorite and silver(I) salts (H.H. Wasserman, 1975). For intramolecular cyclopropane formation see section 1.16. [Pg.77]

N. J. Turro, Modem Molecular Photochemistry, University Science Books, 1991. [Pg.397]

N. Turro, Modern Molecular Photochemistry, The Benjamin/Cummings Publishing Co., 1978. [Pg.371]

Heinrich Rinderknecht Michael G Romanelli John P Schaefer Harry P Schultz J E Shields Robert M Silverstein P S Skell A R Surrey S Swaminathan Nicholas J Turro G E VandfnBerg P S Venkataramani George F Vesley K H Vopel B J Wakefield H W Wanzlick Newton W Werner Emil White G Wittig Wysong... [Pg.147]

Similar data were reported by Turro et al., [62,63] who synthesized a copolymer of AA with 1.5 mol% of 2-[4-(l-pyrene)butanoyl]aminopropenoic acid, 19 and studied the fluorescence quenching with Tl +, Cu2+, and 1 ions in aqueous solution. [Pg.73]

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See also in sourсe #XX -- [ Pg.695 ]

See also in sourсe #XX -- [ Pg.116 , Pg.140 , Pg.147 , Pg.192 , Pg.378 ]

See also in sourсe #XX -- [ Pg.230 ]



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Dauben-Turro-Salem analysis

Dauben-Turro-Salem analysis Norrish type

Dauben-Turro-Salem analysis orbital interaction diagram

Photochemistry Dauben-Salem-Turro

Salem-Turro Analysis

Solution Phase Photochemistry of (Morton and Turro)

State correlation diagrams Dauben-Salem-Turro

Turro studies

Turro, Nicholas

Turro, Nick

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