ChemInform Abstract: PREPARATION OF Δ5-7-OXO STEROIDS BY ALLYLIC OXIDATION OF Δ5 STEROIDS: A STUDY OF THE REACTIVITY OF THE CHROMIUM TRIOXIDE-PYRIDINE 1:1 AND 1:2 COMPLEXES PREPARED IN SITU

1979 ◽  
Vol 10 (28) ◽  
Author(s):  
E. MAPPUS ◽  
C.-Y. CUILLERON
1978 ◽  
Vol 43 (10) ◽  
pp. 2057-2059 ◽  
Author(s):  
William G. Salmond ◽  
Mary A. Barta ◽  
Jeffrey L. Havens

2019 ◽  
Vol 12 (3) ◽  
pp. 1055-1067 ◽  
Author(s):  
Anna Winiwarter ◽  
Luca Silvioli ◽  
Soren B. Scott ◽  
Kasper Enemark-Rasmussen ◽  
Manuel Sariç ◽  
...  

High coverage of the catalyst surface generated by in situ degradation of propene steers the reaction towards allylic oxidation.


1971 ◽  
Vol 36 (23) ◽  
pp. 3657-3657
Author(s):  
William Dauben ◽  
Milton Lorber ◽  
Dwight Fullerton

1973 ◽  
Vol 51 (9) ◽  
pp. 1346-1358 ◽  
Author(s):  
M. S. Henderson ◽  
R. McCrindle ◽  
D. McMaster

Eight new furan-containing diterpenoids from Solidago gigantea Ait. var. serotina (Kuntze) Cronqu., are formulated as 1c–g, 2, 3a, and 4a on the basis of chemical and spectroscopic evidence and by correlation with solidagoic acid A of previously defined constitution and stereochemistry. The structure (5a) of a ninth related compound is tentatively assigned. The allylic oxidation of some of these new diterpenoids and related compounds with the chromium trioxide – pyridine complex is reported. In the course of this investigation of formal total synthesis of compound Y from Leonotis leonurus was achieved.


1969 ◽  
Vol 34 (11) ◽  
pp. 3587-3592 ◽  
Author(s):  
William G. Dauben ◽  
Milton E. Lorber ◽  
Dwight S. Fullerton

1991 ◽  
Vol 69 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Gervais Bérubé ◽  
Alex G. Fallis

A general intramolecular Diels–Alder anionic oxy-Cope strategy for the synthesis of tricyclic skeletons and its application to the preparation of the gascardic acid precursor 21 is described. In situ generation of the appropriate cyclopentadiene 9 by isomerization (Et3N) afforded the [4+2] adduct directly or with EtAlCl2 as catalyst. The requisite potassium salt of the 1,5 diene 16 rearranged with concomitant epimerization at 67 °C to the fused ring ketone 18. Selective allylic oxidation and reduction provided 21. Key words: Diels–Alder, oxy-Cope, sesterterpene, synthesis, cycloaddition.


1985 ◽  
Vol 17 (3) ◽  
pp. 192-194 ◽  
Author(s):  
Edward J. Parish ◽  
Sarawanee Chitrakorn ◽  
Kenneth L. Todd

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