Migration of hydroxyl in secondary systems during solvolysis in acid solution

1977 ◽  
Vol 55 (21) ◽  
pp. 3774-3785 ◽  
Author(s):  
Robert C. Cathcart ◽  
John W. Bovenkamp ◽  
Robert Y. Moir ◽  
Robert A. B. Bannard ◽  
Alfred A. Casselman

A system of compounds has been prepared which is well adapted for displaying the role of trans vicinal, secondary hydroxyl in solvolysis. On methanolysis in acid solution, compounds 5, 7a, and 8a all gave the same products, 9a and 10a, and in practically the same proportions, suggesting that at least one intermediate was common to all three reactions. These intermediates were such that 7a and 8a were not interconverted during the solvolysis, a fact in support of 6 as a common intermediate. Several alternative explanations were shown to be untenable, largely by taking advantage of the remarkable differences between hydroxyl and methoxyl. The work provides the most decisive evidence available for the covalent participation of hydroxyl as a neighbor group in the solvolysis of secondary systems, and contributes also to the study of the reverse reaction, the acid-catalyzed scission of epoxides.

1995 ◽  
Vol 33 (11) ◽  
pp. 1841-1848 ◽  
Author(s):  
Eugène T. W. M. Schipper ◽  
Johan P. A. Heuts ◽  
Ralph P. M. Pinckaers ◽  
Pieter Piet ◽  
Anton L. German
Keyword(s):  

2021 ◽  
pp. 1-11
Author(s):  
Debasree Chanda ◽  
Gangothri M. Venkataswamy ◽  
Lagamawwa V. Hipparagi ◽  
Nanishankar V. Harohally

1952 ◽  
Vol 30 (3) ◽  
pp. 169-176 ◽  
Author(s):  
A. M. Eastham ◽  
G. A. Latremouille

The rates of reaction of halide ions with ethylene oxide in neutral aqueous solution and the rate of hydrolysis of ethylene oxide in acid solution have been measured and the activation energies determined. From these data and from the ratio of glycol to chlorohydrin formed when ethylene oxide reacts with excess aqueous hydrogen halide, the rates of the acid-catalyzed addition of halide ions to ethylene oxide at 25 °C. have been estimated.


2010 ◽  
Vol 5 (5) ◽  
pp. 1934578X1000500
Author(s):  
Jixun Zhan ◽  
E. M. Kithsiri Wijeratne ◽  
A. A. Leslie Gunatilaka

Biotransformation of monocillin I (1) by Beauveria bassiana ATCC 7159 was investigated. Two new derivatives 2 and 3 were isolated and identified on the basis of the spectroscopic data. Compounds 2 and 3 are synthesized by hydration at 10,11-double bond and hydrolysis of 14,15-epoxide, respectively. The R configuration of 11-OH in 2 was established by the modified 2-methoxy-2-trifluoromethylphenylacetic acid (MTPA) method. The conversion of 1 to 2 and 3 was reconstituted in an acid solution, indicating that the formation of 2 and 3 is an acid-catalyzed instead of an enzymatic process.


2020 ◽  
Vol 5 (4) ◽  
pp. 651-662 ◽  
Author(s):  
Gourav Shrivastav ◽  
Tuhin S. Khan ◽  
Manish Agarwal ◽  
M. Ali Haider

Utilizing the differential stabilization of reactant and transition state in the polar and apolar solvents to lower the activation free energy barrier for acid-catalyzed dehydration of hydroxy lactones.


1991 ◽  
Vol 30 (7) ◽  
pp. 1668-1670 ◽  
Author(s):  
Simeen. Sattar ◽  
Kenneth. Kustin

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