Crossed Aldol Reactions of Dioxolans

1989 ◽  
Vol 42 (11) ◽  
pp. 1939 ◽  
Author(s):  
RC Cambie ◽  
PS Rutledge ◽  
PA Watson ◽  
PD Woodgate

The crossed aldol reactions of some cyclohexyl and cyclohexenyl dioxolans with the silyl enol ether of cyclohexanone have, in general, been shown to result in directed opening of the acetal. However, only limited stereoselectivity results at the termini of the new carbon-carbon bond.

1989 ◽  
Vol 54 (11) ◽  
pp. 2605-2608 ◽  
Author(s):  
V. V. Zhdankin ◽  
M. Mullikin ◽  
Rik Tykwinski ◽  
Bruce Berglund ◽  
Ronald Caple ◽  
...  

1988 ◽  
Vol 29 (30) ◽  
pp. 3703-3704 ◽  
Author(s):  
Viktor V. Zhdankin ◽  
Rik Tykwinski ◽  
Ronald Caple ◽  
Bruce Berglund ◽  
Anatoly S. Koz'min ◽  
...  

ChemInform ◽  
1989 ◽  
Vol 20 (47) ◽  
Author(s):  
V. V. ZHDANKIN ◽  
M. MULLIKIN ◽  
R. TYKWINSKI ◽  
B. BERGLUND ◽  
R. CAPLE ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (76) ◽  
pp. 62179-62193 ◽  
Author(s):  
Amrutha P. Thankachan ◽  
S. Asha ◽  
K. S. Sindhu ◽  
Gopinathan Anilkumar

Enantioselective zinc-catalyzed aldol reactions provide an efficient route for the construction of a wide range of carbon–carbon bond-formation, which are described here.


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