A special-salt effect upon the hydride shift during the acetolysis of cyclohexyl tosylate

1976 ◽  
Vol 41 (24) ◽  
pp. 3920-3922 ◽  
Author(s):  
M. Gillard ◽  
F. Metras ◽  
S. Tellier ◽  
J. J. Dannenberg
Keyword(s):  
1977 ◽  
Vol 8 (12) ◽  
pp. no-no
Author(s):  
M. G. GILLARD ◽  
F. METRAS ◽  
S. TELLIER ◽  
J. J. DANNENBERG
Keyword(s):  

1952 ◽  
Vol 44 (3) ◽  
pp. 444-444
Author(s):  
N Chalapathi Rao ◽  
Hugh Winn ◽  
J Shelton

1981 ◽  
Vol 46 (12) ◽  
pp. 3104-3109 ◽  
Author(s):  
Miroslav Ludwig ◽  
Oldřich Pytela ◽  
Miroslav Večeřa

Rate constants of non-catalyzed hydrolysis of 3-acetyl-1,3-diphenyltriazene (I) and 3-(N-methylcarbamoyl)-1,3-diphenyltriazene (II) have been measured in the presence of salts (ammonium chloride, potassium chloride, lithium chloride, sodium chloride and bromide, ammonium sulphate, potassium sulphate, lithium sulphate, sodium sulphate and zinc sulphate) within broad concentration ranges. Temperature dependence of the hydrolysis of the substrates studied has been measured in the presence of lithium sulphate within temperature range 20° to 55 °C. The results obtained have been interpreted by mechanisms of hydrolysis of the studied substances.


1986 ◽  
Vol 51 (12) ◽  
pp. 2781-2785 ◽  
Author(s):  
M. Martín Herrera ◽  
J. J. Maraver Puig ◽  
F. Sánchez Burgos

A study is made on the kinetic salt effect on the reaction of hydrolysis of several charged esters in alkaline media. The results are interpreted on the basis of the coulombic interaction, the salting in of hydroxide ion and a third component depending on size of the substrate.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jianyu Zhang ◽  
Xi Wang ◽  
Tao Xu
Keyword(s):  
Type Ii ◽  

AbstractTo the best of our knowledge, bridgehead carbon benzofused-bridged ring systems have previously not been accessible to the synthetic community. Here, we describe a formal type-II [4 + 4] cycloaddition approach that provides fully sp2-carbon embedded anti-Bredt bicyclo[5.3.1] skeletons through the Rh-catalyzed C1–C8 activation of benzocyclobutenones (BCBs) and their coupling with pedant dienamides. Variously substituted dienamides have been coupled with BCBs to provide a range of complex bicyclo[5.3.1] scaffolds (>20 examples, up to 89% yield). The bridged rings were further converted to polyfused hydroquinoline-containing tetracycles via a serendipitously discovered transannular 1,5-hydride shift/Prins-like cyclization/Schmidt rearrangement cascade.


1998 ◽  
Vol 39 (3) ◽  
pp. 623-632 ◽  
Author(s):  
Martin Wickham ◽  
Martin Garrood ◽  
John Leney ◽  
Peter D.G. Wilson ◽  
Annette Fillery-Travis

Science ◽  
1971 ◽  
Vol 172 (3988) ◽  
pp. 1128-1132 ◽  
Author(s):  
R. C. Bubeck ◽  
W. H. Diment ◽  
B. L. Deck ◽  
A. L. Baldwin ◽  
S. D. Lipton
Keyword(s):  
New York ◽  

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