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16-Substituted steroids

✍ Scribed by R.H. Mazur; J.A. Cella

Book ID: 103397700
Publisher: Elsevier Science
Year: 1959
Tongue: French
Weight: 820 KB
Volume: 7
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(59)80060-0

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📜 SIMILAR VOLUMES

✍ R.H. Mazur; J.A. Cella 📂 Article 📅 1959 🏛 Elsevier Science 🌐 French ⚖ 71 KB

Am-The reactions of 3gJlcetoxy-5,16-pregnadien-20-oM: with cyanide ion and with certain active methylcne compounds are described. Subsequent transformations of the initial products to give various 16-substituted pre&"noiones and progp;&rones are shown.

16-Substituted Steroids. I. Isoestriol-A

✍ Huffman, Max N.; Darby, Hugh H. 📂 Article 📅 1944 🏛 American Chemical Society 🌐 English ⚖ 406 KB

A NOVEL SYNTHESIS OF 16-SUBSTITUTED STER

A NOVEL SYNTHESIS OF 16-SUBSTITUTED STEROIDS

✍ Moreland, Walter T.; Berg, Rudolph G.; Cameron, Donald P. 📂 Article 📅 1960 🏛 American Chemical Society 🌐 English ⚖ 247 KB

Synthesis of 16β-Chlorocortisone Acetate

Synthesis of 16β-Chlorocortisone Acetate and Related 16-Substituted Steroids

✍ BEYLER, R. E.; HOFFMAN, FRANCES. 📂 Article 📅 1956 🏛 American Chemical Society 🌐 English ⚖ 351 KB

16-Substituted Steroids. VIII. 1,3,5(10)

16-Substituted Steroids. VIII. 1,3,5(10)-Estratrien-3-ol-16-one

✍ Huffman, Max N.; Lott, Mary Harriet 📂 Article 📅 1953 🏛 American Chemical Society 🌐 English ⚖ 425 KB

16-Substituted Steroids. X. Androstan-17

16-Substituted Steroids. X. Androstan-17β-ol-3,16-dione

✍ Huffman, Max N.; Lott, Mary Harriet 📂 Article 📅 1954 🏛 American Chemical Society 🌐 English ⚖ 271 KB