Preparation of ethyl diazoacetate via a triazene intermediate

1967 ◽  
Vol 32 (2) ◽  
pp. 484-485 ◽  
Author(s):  
Ronald J. Baumgarten
Keyword(s):  
1996 ◽  
Vol 61 (12) ◽  
pp. 1798-1804 ◽  
Author(s):  
Albert Demonceau ◽  
François Simal ◽  
Corine A. Lemoine ◽  
Alfred F. Noels ◽  
Igor T. Chizhevsky ◽  
...  

The title compound was found to be an efficient catalyst for the selective cyclopropanation of activated olefins by ethyl diazoacetate. The cyclopropane yields range from moderate to good (75 to 95%) for activated olefins such as styrene and styrene derivatives, but are rather low (20 to 30%) for non-activated olefins such as terminal and cyclic alkenes. In the intermolecular competition, styrene was 45 times more reactive than cyclooctene. In all cases, trans (exo) cyclopropane predominated over the cis (endo) isomer.


Author(s):  
Mizzanoor Rahaman ◽  
M. Shahnawaz Ali ◽  
Khorshada Jahan ◽  
Damon Hinz ◽  
Jawad Bin Belayet ◽  
...  

2009 ◽  
Vol 42 (22) ◽  
pp. 8608-8610 ◽  
Author(s):  
Eiji Ihara ◽  
Yasuaki Ishiguro ◽  
Naoki Yoshida ◽  
Toshimitsu Hiraren ◽  
Tomomichi Itoh ◽  
...  
Keyword(s):  

1976 ◽  
Vol 7 (3) ◽  
pp. no-no
Author(s):  
ALAN W. JOHNSON ◽  
DAVID WARD ◽  
PETER BATTEN ◽  
ALAN L. HAMILTON ◽  
GEOFFREY SHELTON ◽  
...  

1974 ◽  
Vol 5 (43) ◽  
pp. no-no
Author(s):  
P. BATTEN ◽  
A. HAMILTON ◽  
A. W. JOHNSON ◽  
G. SHELTON ◽  
D. WARD
Keyword(s):  

1975 ◽  
Vol 40 (10) ◽  
pp. 1527-1528 ◽  
Author(s):  
Timothy B. Patrick ◽  
George H. Kovitch
Keyword(s):  

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