STUDIES ON THE MECHANISMS OF CYCLIZATION OF RING A OF STEROIDS DURING THE REFORMATSKY REACTION
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The Reformatsky reaction of 3,5-seco-5-ketocholestan-3-oic acid methyl ester with methyl bromoacetate yielded 2-carbohydroxycholestenone, cholestenone, and 4-carbomethoxycholestenone. The appearance of these products indicated that cyclization of ring A proceeded along two different paths; this conclusion was confirmed by the use of methyl bromoacetate-1-C14 and -2-C14.
2008 ◽
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2015 ◽
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2015 ◽
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