Nuclear recoil reactions in organomanganese compounds. IV. Fulvalenehexacarbonyldimanganese

1970 ◽  
Vol 48 (10) ◽  
pp. 1614-1615 ◽  
Author(s):  
I. G. DeJong ◽  
D. R. Wiles

The chemical effects of neutron capture have been studied in fulvalenehexacarbonyldimanganese, in order to determine whether or not the ring–ring bond survives nuclear recoil. Retention in the parent form (9.1 %) is comparable to that in other organomanganese compounds, while the radiochemical yield of CpMn(CO)3, the "monomer", is very much lower (0.2%). This suggests that the inter-ring bond is not broken under the conditions in the reaction zone. The formation of radiomanganese compounds with several carbonyl ligands (4.7%) is in accord with mass spectrometric evidence, which suggests that CO may be readily available in the reaction zone.

1981 ◽  
Vol 30 (17) ◽  
pp. 2461-2468 ◽  
Author(s):  
Steven A. Barker ◽  
John A. Monti ◽  
Lelland C. Tolbert ◽  
George B. Brown ◽  
Samuel T. Christian

2017 ◽  
Vol 16 (12) ◽  
pp. 4531-4535 ◽  
Author(s):  
Abidali Mohamedali ◽  
Seong Beom Ahn ◽  
Varun K. A. Sreenivasan ◽  
Shoba Ranganathan ◽  
Mark S. Baker

2017 ◽  
Vol 12 (3) ◽  
pp. 1934578X1701200
Author(s):  
Jabar B.P.A.A. Agbo ◽  
James D.S. Mpetga ◽  
Raphael Bikanga ◽  
Roland T. Tchuenguem ◽  
Rolande B.N. Tsafack ◽  
...  

Three alkaloids including a new one, N-formyldihydrochelerythrine (1), together with four other known compounds were isolated from the stem bark of Caloncoba glauca. The structure of the new compound was elucidated from spectroscopic and mass spectrometric evidence. This is the first report of alkaloids from the genus Caloncoba. Sesamin (4) [MIC = 256 μg/mL ( Candida albicans) and dihydrochelerythrine (2) [MIC = 32 ( C. albicans and C. parapsilosis), and 128 μg/mL ( C. krusei)] had moderate to weak antifungal activity.


1962 ◽  
Vol 24 (7) ◽  
pp. 927-930 ◽  
Author(s):  
D.J. Apers ◽  
F.G. Dejehet ◽  
B.S. van Outryve d'Ydewalle ◽  
P.C. Capron

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