The synthesis of 3H-1,2-diazepines by the base-induced elimination of toluene-p-sulphinic acid from 3,4-dihydro-2-tosyl-1,2-diazepines, and some observations on sigmatropic hydrogen shifts in the 3H-1,2-diazepine system
β Scribed by Anderson, Colin D.; Sharp, John T.; Strathdee, R. Stewart
- Book ID
- 125532836
- Publisher
- Royal Society of Chemistry
- Year
- 1979
- Weight
- 712 KB
- Category
- Article
- ISSN
- 1472-7781
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
o-Nitrophenylazide was treated with the low-valent titanium reagent derived from the TiCl 4 /Sm system to produce the intermediate 2 in situ, which was a 'living' double-anion and reacted readily with ketones containing active methyl or methylene groups to afford 2,3-dihydro-1H-1,5-benzodiazepines i
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v