A New Hydrindanone Synthesis
✍ Scribed by Massimo Curini; Francesco Epifano; Maria Carla Marcotullio; Ornelio Rosati; Yousheng Guan; Ernest Wenkert
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- German
- Weight
- 77 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), a-methylation, subsequent conversion into the diazoethanone 14, and, finally, treatment with dirhodium tetraacetate of which furnished the hydrindanone 1 of the steroid C-D ring structure.
Scheme 1
📜 SIMILAR VOLUMES
Ethyl 1-methyl-2-oxocyclohexanecarboxylate (1a) and its homologue 1b were converted to hydroisobenzofuran acids 7 (via 6-[(butylsulfanyl)methylene] and epoxide derivatives), one of which furnished hexalone derivative 11 (via an intermediate diazomethyl ketone derivative). The above-mentioned startin
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
done for a much smaller (54-atom) crystal of the same shape in order to minimize computation time. Figure 5b shows the computation for an ideal cubeoctahedron containing 55 atoms as viewed along (1 10). Finally, Figures 5c and5d show the image simulations for the bcc structure as viewed along (100)