Photoinduced molecular transformations. Part 107. A versatile substitution of a carbonyl group of steroidal ketones by a heteroatom. The synthesis of aza-, oxa-, thia-, selena-, and tellurasteroids
- 1 March 1990
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 55 (7) , 2170-2176
- https://doi.org/10.1021/jo00294a035
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Cyclization of 3,3;20,20-bis(ethylenedioxy)-C-nor-9,11-seco-5α-pregnane-9β,11-diol into 11-oxa-5α,17α-pregnane-3,20-dioneJournal of the Chemical Society, Perkin Transactions 1, 1986
- Replacement of a Carbonyl Group of Camphor by an Oxygen Atom. Synthesis of 1,7,7-Trimethyl-2-oxabicyclo[2.2.1]heptaneBulletin of the Chemical Society of Japan, 1985
- Steroids and related studies. Part 44. 17a-Methyl-3β-(N-pyrrolidinyl)17a-aza-D-homo-5α-androstane bis(methiodide)(dihydrochandonium iodide) and certain other analogues of chandonium iodideJournal of the Chemical Society, Perkin Transactions 1, 1979