B H Jennings, L M Yelle
Index: Steroids 37(1) , 7-22, (1981)
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A comparative study was made of the reactions of 5-bromo-3 beta, 6 beta-dihydroxy-5 alpha-androstan-17-one 3-acetate (1) with lead tetraacetate alone and in the presence of iodine in both high intensity visible light and in total darkness using a variety of solvents. Markedly different product profiles were obtained under the different reaction conditions, making our results of both practical importance and theoretical interest.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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lead tetraacetate
CAS:546-67-8 |
C8H12O8Pb |
|
Chlorodecarboxylation of 17 beta-acetoxy-3-methoxy-9-oxo-9, ...
1982-05-01 [Steroids 39(5) , 537-45, (1982)] |
|
Formation of an unusual dimeric compound by lead tetraacetat...
2002-07-01 [Chem. Pharm. Bull. 50(7) , 960-3, (2002)] |
|
An efficient synthesis of 4 beta- and 6 alpha-hydroxylated b...
1993-02-01 [Steroids 58(2) , 52-8, (1993)] |
|
Synthesis of c-2, 3, 17 and 19-oxygenated androgens.
1988-03-01 [J. Steroid Biochem. 29(3) , 353-9, (1988)] |
|
A practical preparation of the key intermediate for penems a...
2013-03-01 [J. Antibiot. 66(3) , 161-3, (2013)] |
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