## 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: Generation of the Furan Analogue of ortho-Quinodimethane by 1,4- Elimination of 3-Acetoxymethyl-2-tributylstannylmethylfuran.
β Scribed by G.-B. LIU; H. MORI; S. KATSUMURA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Evidence for a Stepwise Ionic Pathway in the Generation of Indole-2,3-quinodimethanes. -A strategy employing C-2 carbon substitution of (I) by NBS bromination is used for an effective synthesis of the lactone (IV). However, contrary to the previously reported analogues (V) compound (IV) is totally
Synthesis of 2-Alkylidene-3,3-dialkyl-1,4-dithianes and Their Oxathiane Analogues by 1,2-Sulfur Migration. -Base-promoted mesylation of tertiary alcohols such as (I) and (III) derived from dithianes or oxathianes results in rearrangement by sulfur migration to yield the 1,4-dithianes (II) and their
## 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