1,2-O-Isopropylidenefuranose Templates for the Synthesis of Complex Cyclic Ethers via Neighboring Group Participation by the Acetal Ring Oxygen

1994 ◽  
Vol 59 (26) ◽  
pp. 7986-7993 ◽  
Author(s):  
Weifang Shan ◽  
Phyllis Wilson ◽  
Wei Liang ◽  
David R. Mootoo
1981 ◽  
Vol 46 (11) ◽  
pp. 2877-2891 ◽  
Author(s):  
Pavel Kočovský ◽  
František Tureček

Hypobromous acid addition to the diene VII yields two epimeric dibromo 6β,19a-epoxides, XVI (main product) and XVII, via the intermediary bromohydrin XIII. Products due to C-C bond formation were not observed. This fact is attributed to the mutual perpendicular arrangement of π-orbitals of the two double bonds in the diene VII. Hypobromous acid action upon the 5α,6β-diol IX and the dimethoxy derivative X afforded analogous products of 6(O)n participation by the 6β-substituent, i.e. the cyclic ethers XXII, XXIII and XXIV, XXV. Under the same conditions the 6β-acetoxy derivative XI gave a mixture of the cyclic ethers XXII and XXIII as products of 6(O)n participation, and the rearranged ketone XXVI. Mechanism of this rearrangement is discussed.


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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