Allylic rearrangement in reactions of acetylenic compounds with allyl and benzyl derivatives of boron

Author(s):  
B. M. Mikhailov ◽  
Yu. N. Bubnov ◽  
S. A. Korobeinikova
1984 ◽  
Vol 49 (9) ◽  
pp. 2111-2115 ◽  
Author(s):  
Abdel Ghani Ali El-Agamey ◽  
Levan P. Asatiani

1-Ferrocenyl(methyl)phenylsilane (I) was prepared by silylation of ferrocene at low temperature. Mono- and diacetylenic compounds of silyferrocene were prepared by the interaction of chloroferrocenylsilane with mono- and dilithium acetylenic derivatives, respectively. It has been found that, catalytic hydrogenation of the prepared acetylenic compounds seem to be totally determined by steric considerations.


1966 ◽  
Vol 19 (9) ◽  
pp. 1977 ◽  
Author(s):  
EFLJ Anet

The unsaturated ketose, 3,4-dideoxy-D-glycero-hex-trans-3-enulose, was prepared from 3-deoxy-2-O-methyl-β-D-erythro-hex-2-enofuranose by reduction with sodium borohydride followed by an allylic rearrangement under mild acid conditions. Further reduction of the ketose with sodium borohydride yielded erythro- and D-threo-hex-trans-3-ene-1,2,5,6- tetrols. The 1,2:5,6 di-O-isopropylidene derivatives of the tetrols were also prepared. The main evidence for the trans configuration of the double bonds of these five compounds is that they have a large value for J3.4 (15.4-16.4 c/s).


1982 ◽  
Vol 85 (1) ◽  
pp. 257-263 ◽  
Author(s):  
A. Graja ◽  
M. Przybylski ◽  
B. Butka ◽  
R. Swietlik

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