1970
DOI: 10.1002/anie.197003211
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Modern Steroid Problems

Abstract: Dedicated to Professor R. Tschesche on the occasion of his 65th birthdayThe present article is concerned primarily with the latest developments in the fields of steroids exhibiting contraceptive, antiandrogenic, or cardiac activity and of steroid metamorphosis hormones. Both the biological action and the current sources of raw materials are considered.

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Cited by 26 publications
(7 citation statements)
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“…Other phytosterols such as hecogenin and solasodine from Agave and Solanum species, respectively, have been used as well, but to a lesser extent. Furthermore, the utilization of, for instance, tall oil, sugarcane or soybean sterols as an economic source of intermediates for steroid manufacture has been long considered for supplementing or supplanting the commercial processes from diosgenin [24].…”
Section: Discussionmentioning
confidence: 99%
“…Other phytosterols such as hecogenin and solasodine from Agave and Solanum species, respectively, have been used as well, but to a lesser extent. Furthermore, the utilization of, for instance, tall oil, sugarcane or soybean sterols as an economic source of intermediates for steroid manufacture has been long considered for supplementing or supplanting the commercial processes from diosgenin [24].…”
Section: Discussionmentioning
confidence: 99%
“…The realization of this classical diene approach for the estrone synthesis demonstrated the versatility and unique reactivities of the oxabicyclo[2.2.1]heptane template. This strategy could be applicable to the stereocontrolled synthesis of steroids , and relevant terpenoids in general with further development, which we are pursuing in our laboratories.…”
Section: Discussionmentioning
confidence: 99%
“…Phytosterols were deemed to be such a resource. Already in 1970, Wiechert noted that such phytosterols as -sitosterol are regaining importance as raw materials for steroidal hormones due to the fact that enzymatic degradations of the C-17 side chain of phytosterols became better understood 66 . Scheme 24.…”
Section: Enzymatic Cleavage Of the C17-side Chain In Cholesterol Sito...mentioning
confidence: 99%