1989
DOI: 10.1016/0022-4731(89)90248-3
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Evidence of formation of isomeric methoximes from 20-oxosteroids

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Cited by 5 publications
(2 citation statements)
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“…I(c) and l(d), giving syn-and anti-components easily resolved by GC. Oximes at C-20 of steroids containing an adjacent C-17 a-hydroxyl group do not show geometrical isomerism (Bournot and Ramirez 1989). Analogous GC-MS studies of steroidal oxime TMS ethers have been reported for free and conjugated steroids in ovarian fluids of catfish (Schoonen et al 1989).…”
Section: Discussionmentioning
confidence: 88%
“…I(c) and l(d), giving syn-and anti-components easily resolved by GC. Oximes at C-20 of steroids containing an adjacent C-17 a-hydroxyl group do not show geometrical isomerism (Bournot and Ramirez 1989). Analogous GC-MS studies of steroidal oxime TMS ethers have been reported for free and conjugated steroids in ovarian fluids of catfish (Schoonen et al 1989).…”
Section: Discussionmentioning
confidence: 88%
“…Tordanone (78), a doubly-bent steroid having both rings A/B and B/C cis-fused, has been prepared by stereospecific hydrogenation of the dienone (79). 48 There is severe steric hindrance on the p-face, where the angular methyl group at the C/D ring junction is in compression with the 7P-hydrogen of ring B.…”
Section: Other Reactions Of Olefinic and Aromatic Steroidsmentioning
confidence: 99%