Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Scott T. Hill"'
1
Cp*Ru+ complexes of benzylideneaniline and salicylideneaniline
Autor: Dale E Wheeler, Scott T. Hill, Kraig A. Luczak, Steven Milos, Grant N. Holder, Nicholas W Baetz
Publikováno v: Inorganica Chimica Acta. 328:210-217
The reaction product of Cp*Ru(CH 3 CN) 3 + OSO 2 CF 3 − with salicylaldehyde yielded ( 1 ) which reacted with a series of aniline derivatives to produce air-stable solids. These products were characterized by 1 H and 13 C NMR spectrometry and UV–
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8dd3a90cd8980fade31b3035d47b3606
https://doi.org/10.1016/s0020-1693(01)00733-2
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2
Reactions of Cp* Ru(η6-C6H5CHO)+ OSO2CF3− (Cp* = C5Me5) with substituted anilines forming ruthenium Schiff base complexes
Autor: Dale E. Wheeler, Scott T. Hill, Steven Milos, Jason D. Johnson, John D. Williams
Publikováno v: Journal of Organometallic Chemistry. 530:83-87
Cp * Ru(η 6 -C 6 H 5 CHO) + OSO 2 CF 3 − ( 1 ) (Cp * = C 5 Me 5 ) reacts with substituted anilines forming ruthenium Schiff base complexes containing an η 6 -coordinated Cp * Ru + group. The 2:1 reaction of 1 with 1,4-phenylenediamine yielded onl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6da706170a05ac74140a7ec06bf1a944
https://doi.org/10.1016/s0022-328x(96)06587-4
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3
Coordination site preference study of Cp∗Ru+ in monosubstituted naphthalene complexes
Autor: Dale E. Wheeler, John M. Carey, Scott T. Hill
Publikováno v: Inorganica Chimica Acta. 249:157-161
Ten novel [Cp ∗ Ru(η 6 -monosubstituted naphthalene) + O 3 SCF 3 − complexes were synthesized and characterized by 1 H, 13 C and 1 H{ 1 H}-COSY NMR spectrometry. All complexes containing electron-withdrawing substituents formed products with Cp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::81effaa66cb111e5e988a7b79aa7b2bf
https://doi.org/10.1016/0020-1693(96)05091-8
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4
Cyclopentene Synthesis from 1,3-Dienes via Base-Induced Ring Contraction of 3,6-Dihydro-2H-thiopyrans: Studies on Diastereoselection and Mechanism
Autor: Brian E. Libby, Scott D. Larsen, Peter V. Fisher, Warren R. Ronk, W. Watt, Scott T. Hill, Stephen A. Mizsak, Randy M. Jensen
Publikováno v: The Journal of Organic Chemistry. 61:4725-4738
An investigation of the scope and mechanism of a new synthesis of cyclopentenes from 3,6-dihydro-2H-thiopyrans is described. Alkyl halides substituted with an electron-withdrawing group in the alpha-position were reacted with sodium thiosulfate, yiel
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc936dd93d6330325ae5e5f683ea60c3
https://doi.org/10.1021/jo960537o
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5
Synthesis and characterization of and complexes
Autor: Scott T. Hill, Dale E. Wheeler, Elisa J. Wedyck, John D. Williams
Publikováno v: Inorganica Chimica Acta. 231:133-138
Eight novel [ Cp ∗ Ru η 6 - arene )] + O 3 SCF 3 − complexes and eight novel [ Cp ∗ Ru (η 6 :η 6 - diarene ) RuCp ∗ ] 2+ 2[ O 3 SCF 3 − ] complexes (where Cp ∗ = C 5 (CH 3 ) 5 ) were synthesized and characterized by 1H and 13C NMR spec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::201bc138d259561a9d0e2f6cba74536a
https://doi.org/10.1016/0020-1693(94)04345-v
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6
ChemInform Abstract: Cyclopentene Synthesis from 1,3-Dienes via Base-Induced Ring Contraction of 3,6-Dihydro-2H-thiopyrans: Studies on Diastereoselection and Mechanism
Autor: Brian E. Libby, Stephen A. Mizsak, Scott D. Larsen, Peter V. Fisher, Scott T. Hill, W. Watt, Warren R. Ronk, Randy M. Jensen
Publikováno v: ChemInform. 27
An investigation of the scope and mechanism of a new synthesis of cyclopentenes from 3,6-dihydro-2H-thiopyrans is described. Alkyl halides substituted with an electron-withdrawing group in the α-position were reacted with sodium thiosulfate, yieldin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::890cdce80e34d9fa1e64853b06f2a632
https://doi.org/10.1002/chin.199646084
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7
Azabicyclo chemistry.7. Ultra-high field (600 MHz) NMR spectroscopy in solving conformational problems: cis-Octahydroindoles
Autor: Scott T. Hill, Michael Mokotoff
Publikováno v: Journal of Heterocyclic Chemistry. 25:65-71
Studies using ultra-high field (600 MHz) nmr spectroscopy has allowed us to assign the conformational preference of cis-octahydroindoles, including the position of their nitrogen lone-pair electrons. Lithium aluminum hydride reduction of cis-octahydr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::511fdac69565ca9e42374c8d37ba78d6
https://doi.org/10.1002/jhet.5570250110
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