## 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
ChemInform Abstract: Diquinane Synthesis Based on Anionic (1, 3) Sigmatropic Rearrangements of an Oxy-Cope System Incorporated in the Bicyclo(3.2.1)oct-6-ene Framework.
β Scribed by K. SEKI; W. KIYOKAWA; H. HASHIMOTO; T. UYEHARA; M. UENO; T. SATO
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Diquinane Synthesis Based on Anionic (1, 3) Sigmatropic Rearrangements of an Oxy-Cope System Incorporated in the Bicyclo(3.2.1)oct-6-ene Framework. -Treatment of 2-vinylbicyclooctenols (I) and (V) with KH in an appropriate solvent results in the formation of the (5-5) fused-ring compounds (II) and (III) via an anionic (1, 3) migration of the oxy-Cope system. -(SEKI, K.
π SIMILAR VOLUMES
Stereoconvergent Approach to Each of the Stereoisomeric Hydroxydiquinanes Based on the Anionic [1,3] Rearrangement of Bicyclo[3.2.1]oct-6-en-2-ols. -The anionic [1,3] rearrangement of both stereoisomeric bicyclo-octenols (I) and (IV) by treatment with KN(Tms) 2 in toluene or diglyme takes place as
## 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