Mechanism of the reaction of 1-tert-butyl-3-azetidinyl tosylate with methanolic potassium cyanide and with solvent

Robert H. Higgins; Fred M. Behlen; Douglas F. Eggli; James H. Kreymborg; Norman H. Cromwell

doi:10.1021/jo00968a053

Mechanism of the reaction of 1-tert-butyl-3-azetidinyl tosylate with methanolic potassium cyanide and with solvent

The Journal of Organic Chemistry ◽

10.1021/jo00968a053 ◽

1972 ◽

Vol 37 (3) ◽

pp. 524-526 ◽

Cited By ~ 5

Author(s):

Robert H. Higgins ◽

Fred M. Behlen ◽

Douglas F. Eggli ◽

James H. Kreymborg ◽

Norman H. Cromwell

Keyword(s):

Potassium Cyanide ◽

Tert Butyl ◽

Mechanism Of The Reaction

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ChemInform Abstract: CHLORINATION AND S-OXIDATION OF BENZO(B)THIOPHENE WITH TERT-BUTYL HYPOCHLORITE. MECHANISM OF THE REACTION

Chemischer Informationsdienst ◽

10.1002/chin.197818169 ◽

1978 ◽

Vol 9 (18) ◽

Author(s):

P. GENESTE ◽

J. L. OLIVE ◽

S. N. UNG

Keyword(s):

Tert Butyl ◽

S Oxidation ◽

Mechanism Of The Reaction

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171. A criterion for the mechanism of the reaction between alkyl halides and hydroxylic solvents. Reactions of tert.-butyl chloride

Journal of the Chemical Society (Resumed) ◽

10.1039/jr9380000881 ◽

1938 ◽

pp. 881 ◽

Cited By ~ 8

Author(s):

Leslie C. Bateman ◽

Edward D. Hughes ◽

Christopher K. Ingold

Keyword(s):

Alkyl Halides ◽

Butyl Chloride ◽

Tert Butyl ◽

Tert Butyl Chloride ◽

Mechanism Of The Reaction

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On the mechanism of the reaction of ozone with tert-butyl hydroperoxide: 1,3-dipolar insertion, electron-transfer, or molecule-assisted homolysis.

Tetrahedron Letters ◽

10.1016/s0040-4039(01)85370-3 ◽

1978 ◽

Vol 19 (8) ◽

pp. 697-700 ◽

Cited By ~ 5

Author(s):

William A. Pryor ◽

Michael E. Kurz

Keyword(s):

Electron Transfer ◽

Butyl Hydroperoxide ◽

Tert Butyl ◽

Tert Butyl Hydroperoxide ◽

Mechanism Of The Reaction

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Composition of products and mechanism of the reaction of ozone with 2,6-di(tert-butyl)-4-methylphenol

Bulletin of the Russian Academy of Sciences Division of Chemical Science ◽

10.1007/bf00864545 ◽

1992 ◽

Vol 41 (5) ◽

pp. 949-952

Author(s):

S. D. Razumovskii ◽

M. L. Konstantinova ◽

G. E. Zaikov

Keyword(s):

Tert Butyl ◽

Composition Of Products ◽

Mechanism Of The Reaction

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Vicinal Substituted Resorcinols. III. Extension of the Reaction between m-Dinitrobenzene, Potassium Cyanide and Methanol to Other Alcohols. The Mechanism of the Reaction

Journal of the American Chemical Society ◽

10.1021/ja01252a037 ◽

1943 ◽

Vol 65 (12) ◽

pp. 2379-2380 ◽

Cited By ~ 1

Author(s):

Alfred Russell ◽

L. M. Addison

Keyword(s):

Potassium Cyanide ◽

Mechanism Of The Reaction

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Silylation of N,N-bis(2-aminoethyl)ethane-1,2-diamine (TREN) using tert-butyl(chloro)dimethylsilane (TBSCl) and subsequent tri-lithiation

ChemSpider Synthetic Pages ◽

10.1039/sp2 ◽

2001 ◽

Author(s):

Peter Scott

Keyword(s):

Tert Butyl

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A mechanism of mitochondrial damage induced by tert-butyl hydroperoxide and microsomes in vitro

Physiologia Plantarum ◽

10.1034/j.1399-3054.1990.800210.x ◽

1990 ◽

Vol 80 (2) ◽

pp. 226-232

Author(s):

Tomoaki Matsuo ◽

Yumiko Kashiwaki ◽

Saburo Itoo

Keyword(s):

Mitochondrial Damage ◽

Butyl Hydroperoxide ◽

Tert Butyl ◽

Tert Butyl Hydroperoxide

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Dependence of Platelet Adenyl Cyclase System on Oxidative Phosphorylation

Thrombosis and Haemostasis ◽

10.1055/s-0038-1651444 ◽

1975 ◽

Vol 34 (01) ◽

pp. 042-049 ◽

Cited By ~ 1

Author(s):

Shuichi Hashimoto ◽

Sachiko Shibata ◽

Bokro Kobayashi

Keyword(s):

Cyclic Amp ◽

Oxidative Phosphorylation ◽

Sodium Succinate ◽

Potassium Cyanide ◽

Adenyl Cyclase ◽

Mitochondrial Oxidative Phosphorylation ◽

Adenyl Cyclase Activity ◽

Intact Rabbit ◽

Adenyl Cyclase System ◽

Cyclic Amp Synthesis

SummaryThe radioactive adenosine 3′,5′-monophosphate (cyclic AMP) level derived from 8-14C adenine in intact rabbit platelets decreased in the presence of mitochondrial inhibitor (potassium cyanide) or uncoupler (sodium azide), and markedly increased by the addition of NaF, monoiodoacetic acid (MIA), or 2-deoxy-D-glucose. The stimulative effect of the glycolytic inhibitors was distinctly enhanced by the simultaneous addition of sodium succinate. MIA did neither directly stimulate the adenyl cyclase activity nor inhibit the phosphodiesterase activity. These results suggest that cyclic AMP synthesis in platelets is closely linked to mitochondrial oxidative phosphorylation.

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