Mechanisms of nucleophilic reactions of carbonyl compounds in the gas phase and in a solution

A. N. Isaev

doi:10.1007/bf00695811

Mechanisms of nucleophilic reactions of carbonyl compounds in the gas phase and in a solution

Russian Chemical Bulletin ◽

10.1007/bf00695811 ◽

1994 ◽

Vol 43 (2) ◽

pp. 206-208

Author(s):

A. N. Isaev

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

Nucleophilic Reactions

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Trends in Alkyl Substituent Effects on Nucleophilic Reactions of Carbonyl Compounds: Gas-Phase Reactions between Amines and the Methoxy Methyl Cation

European Journal of Mass Spectrometry ◽

10.1255/ejms.533 ◽

2004 ◽

Vol 10 (2) ◽

pp. 233-238 ◽

Cited By ~ 1

Author(s):

Lihn Bache-Andreassen ◽

Einar Uggerud

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

Substituent Effects ◽

Alkyl Substituent ◽

Gas Phase Reactions ◽

Nucleophilic Reactions ◽

Methyl Cation

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Semiempirical and ab initio calculations on geometry and stability of intermediates. Stability of intermediates for nucleophilic reactions of carbonyl compounds in the gas phase and in solution

Journal of Molecular Structure THEOCHEM ◽

10.1016/0166-1280(85)85023-5 ◽

1985 ◽

Vol 133 ◽

pp. 263-268 ◽

Cited By ~ 9

Author(s):

Konstantin Ya. Burshtein ◽

Alexander N. Isaev

Keyword(s):

Ab Initio Calculations ◽

Ab Initio ◽

Gas Phase ◽

Carbonyl Compounds ◽

Nucleophilic Reactions

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Trends in alkyl substituent effects on nucleophilic reactions of carbonyl compounds: Gas phase reactions between ammonia and R1R2COCH3+ oxonium ionsElectronic supplementary information (ESI) available: proton affinities, geometries and energies of optimised structures, structures of the stationary points and a plot of experimental and RRKM ln(kae/ksub) against a-stabilisation constants. See http://www.rsc.org/suppdata/ob/b2/b209955c/

Organic & Biomolecular Chemistry ◽

10.1039/b209955c ◽

2003 ◽

Vol 1 (4) ◽

pp. 705-713 ◽

Cited By ~ 5

Author(s):

Lihn Bache-Andreassen ◽

Einar Uggerud

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

Substituent Effects ◽

Alkyl Substituent ◽

Stationary Points ◽

Supplementary Information ◽

Proton Affinities ◽

Gas Phase Reactions ◽

Nucleophilic Reactions

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Carbonyl Compounds in the Gas Phase of Cigarette Mainstream Smoke and Their Pharmacological Properties

Biological and Pharmaceutical Bulletin ◽

10.1248/bpb.b16-00025 ◽

2016 ◽

Vol 39 (6) ◽

pp. 909-914 ◽

Cited By ~ 20

Author(s):

Takahiro Horinouchi ◽

Tsunehito Higashi ◽

Yuichi Mazaki ◽

Soichi Miwa

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

Pharmacological Properties ◽

Mainstream Smoke ◽

Cigarette Mainstream Smoke

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ChemInform Abstract: GAS PHASE PROTON AFFINITIES OF CARBONYL COMPOUNDS BY ION CYCLOTRON RESONANCE SPECTROSCOPY

Chemischer Informationsdienst ◽

10.1002/chin.197333108 ◽

1973 ◽

Vol 4 (33) ◽

pp. no-no

Author(s):

PAULO C. ISOLANI ◽

JOSE M. RIVEROS ◽

PETER W. TIEDEMANN

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

Cyclotron Resonance ◽

Resonance Spectroscopy ◽

Ion Cyclotron Resonance ◽

Proton Affinities ◽

Ion Cyclotron

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Kurzzeitpyrolyse, VI Ringverengungen durch CO-Eliminierung aus cyclischen Carbonylverbindungen / Short Time Pyrolysis, VI Ring Contractions by CO-Elimination from Cyclic Carbonyl Compounds

Zeitschrift für Naturforschung B ◽

10.1515/znb-1977-0717 ◽

1977 ◽

Vol 32 (7) ◽

pp. 805-806 ◽

Cited By ~ 11

Author(s):

Gerhard Schaden

Keyword(s):

Gas Phase ◽

Carbonyl Compounds ◽

One Step ◽

Short Time

An one-step synthesis of benzocyclobutene (2) by gas-phase pyrolysis of indane-2-one (1) has been found. By the same method indane-1-one (3) and naphthoquinone(1,4) (5) gave indene-1 -one (4) and fluorene-9-one (7) formed biphenylene (8).

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ChemInform Abstract: NUCLEOPHILIC REACTIONS OF ANIONS WITH PF3 AND OPF3 IN THE GAS PHASE BY ION CYCLOTRON RESONANCE SPECTROSCOPY

Chemischer Informationsdienst ◽

10.1002/chin.197835030 ◽

1978 ◽

Vol 9 (35) ◽

Author(s):

S. A. SULLIVAN ◽

J. L. BEAUCHAMP

Keyword(s):

Gas Phase ◽

Cyclotron Resonance ◽

Resonance Spectroscopy ◽

Ion Cyclotron Resonance ◽

Nucleophilic Reactions ◽

Ion Cyclotron

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Nucleophilic reactions of trifluoromethyl ion (F3C-) at sp2 and sp3 carbon in the gas phase. Characterization of carbonyl addition adducts

Journal of the American Chemical Society ◽

10.1021/ja00363a010 ◽

1983 ◽

Vol 105 (25) ◽

pp. 7267-7271 ◽

Cited By ~ 14

Author(s):

Richard N. McDonald ◽

A. Kasem Chowdhury

Keyword(s):

Gas Phase ◽

Nucleophilic Reactions ◽

Carbonyl Addition ◽

Phase Characterization

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Nucleophilic reactions of anions with PF3 and OPF3 in the gas phase by ion cyclotron resonance spectroscopy

Inorganic Chemistry ◽

10.1021/ic50184a039 ◽

1978 ◽

Vol 17 (6) ◽

pp. 1589-1595 ◽

Cited By ~ 9

Author(s):

S. A. Sullivan ◽

J. L. Beauchamp

Keyword(s):

Gas Phase ◽

Cyclotron Resonance ◽

Resonance Spectroscopy ◽

Ion Cyclotron Resonance ◽

Nucleophilic Reactions ◽

Ion Cyclotron

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Electron transfer as a possible initial step in nucleophilic addition elimination reactions between (radical) anions and carbonyl compounds in the gas phase

Recueil des Travaux Chimiques des Pays-Bas ◽

10.1002/recl.19961150304 ◽

2010 ◽

Vol 115 (3) ◽

pp. 179-184 ◽

Cited By ~ 6

Author(s):

Paul O. Staneke ◽

Steen Ingemann ◽

Nico M. M. Nibbering

Keyword(s):

Electron Transfer ◽

Gas Phase ◽

Carbonyl Compounds ◽

Nucleophilic Addition ◽

Initial Step ◽

Radical Anions ◽

Elimination Reactions

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