Concave Reagents,22. Cyclopropanation of Alkenes with Ethyl Diazoacetate: Copper(I) Complexes of Concave 1,10-Phenanthrolines as Diastereoselective Catalysts

1997 ◽  
Vol 130 (2) ◽  
pp. 231-234 ◽  
Author(s):  
Martin Hagen ◽  
Ulrich Lünig
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.


ChemInform ◽  
1990 ◽  
Vol 21 (15) ◽  
Author(s):  
U. LUENING ◽  
R. BAUMSTARK ◽  
M. MUELLER ◽  
C. WANGNICK ◽  
F. SCHILLINGER

ChemInform ◽  
2010 ◽  
Vol 28 (10) ◽  
pp. no-no
Author(s):  
U. LUENING ◽  
H. BAUMGARTNER ◽  
C. MANTHEY ◽  
B. MEYNHARDT

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

1991 ◽  
Vol 124 (2) ◽  
pp. 397-402 ◽  
Author(s):  
Ulrich Lüning ◽  
Carsten Wangnick ◽  
Karl Peters ◽  
Hans Georg Von Schnering

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 ◽  
...  

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