Synthesis of 2-Azulenyl-1,1,4,4-tetracyano-3-ferrocenyl-1,3-butadienes by [2+2] Cycloaddition of (Ferrocenylethynyl)azulenes with Tetracyanoethylene
نویسندگان
چکیده
منابع مشابه
Ferrocenyl substituted chlorostilbenes and butadienes
The readily accessible -chlorophosphonates (OCH2CMe2CH2O)P(O)CH(Cl) C6H4-4-R [1: R=Me (a), OMe (b), Cl (c), H (d)] react with ferrocenecarboxaldehyde in the presence of NaH [Horner–Wadsworth–Emmons reaction] to give good yields of ferrocenyl substituted chlorostilbenes. The novel bis ferrocenyl butadiene C5H5FeC5H4 CH CH C(CN)CHC5H4FeC5H5 (9) as well as the ferrocenyl 2-cyano-1,3-butadienes 4-R...
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synthesis of some new monocyclic β-lactams containing a quaternary carbon center via a [2+2]cycloaddition reaction is described. the reaction of achiral diphenyl ketene with chiral aldimines derivedfrom chiral 2, 3, 4, 6-tetra-o-acetyl-β-d-galactopyranosylamine, 2, 3, 4, 6-tetra-o-acetyl-β-dglucopyranosylamine and different benzaldehydes resulted in the formation of β-lactams as singlediastereo...
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in this thesis, a better reaction conditions for the synthesis of spirobarbiturates catalyzed by task-specific ionic liquid (2-hydroxy-n-(2-hydroxyethyl)-n,n-dimethylethanaminium formate), calcium hypochlorite ca(ocl)2 or n-bromosuccinimide (nbs) in the presence of water at room temperature by ultrasonic technique is provided. the design and synthesis of spirocycles is a challenging task becaus...
15 صفحه اولSynthesis of multisubstituted phenols by formal [4 + 2] cycloaddition of nucleophilic alkynes with 3-ethoxycyclobutanones.
Nucleophilic alkynes bearing sulfonamide, trimethylsilyl, or p-methoxyphenyl groups at the sp carbon reacted with 3-ethoxycyclobutanones to give formal [4 + 2] cycloadducts by activation with TiCl4. Reactions with 2-monoalkyl and 2-nonsubstituted 3-ethoxycyclobutanones gave phenol derivatives directly by benzannulation, while the use of 2,2-dimethyl-3-ethoxycyclobutanone gave the corresponding ...
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ژورنال
عنوان ژورنال: Chemistry - A European Journal
سال: 2013
ISSN: 0947-6539
DOI: 10.1002/chem.201202257