נגישות
menu      
Advanced Search
Syntax
Search...
Volcani treasures
About
Terms of use
Manage
Community:
אסיף מאגר המחקר החקלאי
Powered by ClearMash Solutions Ltd -
The photoalkylation of cyclic ethers
Year:
1967
Source of publication :
Tetrahedron
Authors :
Rosenthal, Ionel
;
.
Volume :
23
Co-Authors:
Rosenthal, I., Daniel Sieff Research Institute, The Weizmann Institute of Science, Rehovoth, Israel
Elad, D., Daniel Sieff Research Institute, The Weizmann Institute of Science, Rehovoth, Israel
Facilitators :
From page:
3193
To page:
3204
(
Total pages:
12
)
Abstract:
The acetone, acetophenone and benzophenone-initiated photochemical alkylation of cyclic ethers with olefins is described. Alpha-alkylated cyclic ethers were obtained as the 1:1-adducts in yields of up to 40% with terminal olfeins, and yields of up to 82% with α,β-unsaturated esters. © 1967.
Note:
Related Files :
Show More
Related Content
More details
DOI :
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
24665
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:09
Scientific Publication
The photoalkylation of cyclic ethers
23
Rosenthal, I., Daniel Sieff Research Institute, The Weizmann Institute of Science, Rehovoth, Israel
Elad, D., Daniel Sieff Research Institute, The Weizmann Institute of Science, Rehovoth, Israel
The photoalkylation of cyclic ethers
The acetone, acetophenone and benzophenone-initiated photochemical alkylation of cyclic ethers with olefins is described. Alpha-alkylated cyclic ethers were obtained as the 1:1-adducts in yields of up to 40% with terminal olfeins, and yields of up to 82% with α,β-unsaturated esters. © 1967.
Scientific Publication
You may also be interested in