Sodium borohydride reduction of carbon monoxide in the cationic iron carbonyl complexes [C5Me5Fe(CO)2L]+ PF6- (L = CO or phosphine)

1988 ◽  
Vol 7 (8) ◽  
pp. 1683-1691 ◽  
Author(s):  
Claude. Lapinte ◽  
Daniel. Catheline ◽  
Didier. Astruc
1964 ◽  
Vol 42 (8) ◽  
pp. 1811-1816 ◽  
Author(s):  
Alex Rosenthal ◽  
Derek Abson

3,4-Di-O-acetyl-D-xylal reacted with carbon monoxide and hydrogen in the presence of dicobalt octacarbonyl to yield 1,5-anhydro-4-deoxy-D-arabino-hexitol (I) and 1,5-anhydro-4-deoxy-L-xylo-hexitol (II). The stereochemistry at C-5 of the hexitols was elucidated by correlation with the triol ether (VI) obtained by sodium borohydride reduction of the periodate oxidation product of 1,4-anhydro-5-deoxy-D-arabino-hexitol (VII). Reaction of 3,4-di-O-acetyl-D-xylal with carbon monoxide and deuterium afforded 1,5-anhydro-4-deoxy-D-arabino-hexitol-4,6,6-H32 (VIII) and 1,5-anhydro-4-deoxy-L-xylo-hexitol-4,6,6-H32 (IX). Examination of the nuclear magnetic resonance (n.m.r.) spectra of the normal and deuterated anhydrodeoxyhexitols confirmed the structural assignments and showed that cis-addition to the double bond takes place to give (IX).


1965 ◽  
Vol 30 (7) ◽  
pp. 2241-2246 ◽  
Author(s):  
Harold Zinnes ◽  
Roger A. Comes ◽  
Francis R. Zuleski ◽  
Albert N. Caro ◽  
John Shavel

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