Reactivity of some steroidal tertiary amines and their derivatives
β Scribed by R. Ledger; J. McKenna; P.B. Smith
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 176 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
IN the Table are listed approtidmate first. order rate constants for the folloting pseudo-unimoleoular reactions: (a), the quaterhisation of some j-dimethylaminocholestanes in a large excess of neat methyl iodide at 21' (kq); (b) the conversion of the resultant trimethylammonium salts and also of two txiethylammonium salts into steroidal olefin (kh,) and steroidal tertiary base () in a large excess of 2Nalcoholic potassium hydrozdde at 83'.
π SIMILAR VOLUMES
1,2-cyclic 3-O-ethyl-and 3-O-hexadecyl-rac-glycerothiophosphates of dehydroisoandrosterone, 13-sitosterol and cholesterol were used as synthons for the preparation of derivatives of phosphocholine and a homologue by alkylation with trimethylamine and triethylamine. The reaction was accomplished eith