An Overview of Water‐Mediated Alkyne Functionalization by Neighboring Group Participation of Carbonyl Groups

2020 ◽  
Vol 362 (22) ◽  
pp. 4833-4860
Author(s):  
Tapas R. Pradhan ◽  
Jin Kyoon Park
1982 ◽  
Vol 47 (1) ◽  
pp. 117-123 ◽  
Author(s):  
Pavel Kočovský ◽  
František Tureček ◽  
Václav Černý

Mechnism of hydrobromous acid addition to 2,3- and 5,6-unsaturated steroids bearing a 19-acetoxy group were established by means of isotopic labeling. In the cleavage of 2α,3α-bromonium ion III participation by the 19-acetoxyl predominates over external attack, 5(O)n process being the major (88%) and 7(O)π,n process the minor (10%) reaction. The external attack by water contributes only 2%. The 5α,6α-bromonium ion XI is cleaved by participation of the 19-acetoxyl at C(5) in a 6(O)π,n process (78%) via XII - XIII. Cleveage at C(6) leads to XIV and occurs partially with 7(O)π,n participation by the 19-acetoxyl (4%) and partially by external attack of water (8%). These results bring evidence for the formation of a seven-membered acetoxonium ion ring as intermediate in participation processes involving ester carbonyl groups.


1982 ◽  
Vol 47 (11) ◽  
pp. 3062-3076 ◽  
Author(s):  
Václav Černý ◽  
Pavel Kočovský

Reactions of the title compounds (bearing an OH, OCH3 or OCOCH3 group at C(19)) involve 5(O)n, 7(O)π,n-participation by the 19-substituent or attack by an external nucleophile. The 6(O)π,n-participation does not occur. The behavior of 1,2-unsaturated (or epoxidated) compounds has been compared with the earlier described 2,3-unsaturated or epoxidated analogs. The 1,2-type is genarally less prone to participation. The reasons for this behavior are discussed.


1982 ◽  
Vol 47 (1) ◽  
pp. 124-129 ◽  
Author(s):  
Pavel Kočovský ◽  
František Tureček ◽  
Václav Černý

The mechanism of perchloric acid cleavage of epoxides I and II was established on the basis of experiments using H2 18O. The 2α,3α-epoxide I gave two products: the cyclic ether V (60%) arising by 5(O)n participation of the 19-acetoxyl and the diol VI (40%). The latter compound is formed by two mechanisms: 1) By direct cleavage of the oxirane ring with H2 18O as external nucleophile and 2) by 7(O)π,n participation via the ion III. Under the same conditions the 5α,6α-epoxide II yielded two diols: The diequatorial diol VIII (96%) arising by 6(O)π,n participation and the diaxial diol IX which is again formed by both direct cleavage of the oxirane ring with H2 18O and by 7(O)π,n participation via the intermediate ion X. The competition of several mechanisms is discussed.


ChemInform ◽  
2010 ◽  
Vol 25 (49) ◽  
pp. no-no
Author(s):  
Y. HASHIMOTO ◽  
Y. SATO ◽  
N. TAKESHITA ◽  
K. KUDO ◽  
K. SAIGO

1988 ◽  
Vol 53 (21) ◽  
pp. 5192-5192
Author(s):  
Sabine Mahling ◽  
Klaus Dieter Asmus ◽  
Richard S. Glass ◽  
Massoud Hojjatie ◽  
Mahmaad Sabahi ◽  
...  

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