5] octane-1,1,2,2-tetracarbonitrile in Synthesis of Heterocyclic Compounds of 2,3-Dihydrofuran and 5,6,7,8-Tetrahydro-4H-chromene Series. -Reaction of tetracyanoethylene (I) with 2-bromodimedone (II) affords the tetracyanospiro[2.5]octane (III) in high yield. On reaction with alcohols or oximes (I
6,6-Dimethyl-4,8-dioxospiro[2.5]octane-1,1,2,2-tetracarbonitrile in the synthesis of heterocyclic compounds of the 2,3-dihydrofuran and 5,6,7,8-tetrahydro-4h-chromene series
β Scribed by O. V. Kayukova; P. M. Lukin; Ya. S. Kayukov; O. E. Nasakin; V. N. Khrustalev; V. N. Nesterov; M. Yu. Antipin
- Publisher
- Springer US
- Year
- 1998
- Tongue
- English
- Weight
- 562 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0009-3122
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## 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 βFull Textβ option. The original article is trackable v
2-Amino-8-oxo-tetrahydro-4H-chromene-3-carbonitriles were synthesized for the first time from a tandem Michael addition - cyclization reaction between cyclohexane-1,2-dione and benzylidenemalononitriles. An enantioselective synthesis of these compounds was achieved in moderate ee values (up to 63% e
## Abstract For Abstract see ChemInform Abstract in Full Text.