منابع مشابه
Palladium-catalyzed multicomponent synthesis of 2-imidazolines from imines and acid chlorides.
We describe the palladium-catalyzed multicomponent synthesis of 2-imidazolines. This reaction proceeds via the coupling of imines, acid chlorides and carbon monoxide to form imidazolinium carboxylates, followed by a decarboxylation. Decarboxylation in CHCl(3) is found to result in a mixture of imidazolinium and imidazolium salts. However, the addition of benzoic acid suppresses aromatization, a...
متن کاملReactions of Atomic Carbon with Acid Chlorides
1his thesis is the flfst report of reactions of atomic calbon with acid chlorides. Carbon is known to react with phosgene to afford dichlorocarbene. We report a similar reaction with carbon and acid ch~lorides, generating alkylchlorocarbenes. We examine both the nature of the carbene products generated through deoxygenation and the general reacliviry ofcarbon with the acid chlorides. We report ...
متن کاملAddition of grignard reagents to aryl acid chlorides: an efficient synthesis of aryl ketones.
[chemical reaction: see text]. Direct addition of Grignard reagents to acid chlorides in the presence of bis[2-(N,N-dimethylamino)ethyl] ether proceeds selectively to provide aryl ketones in high yields. A possible tridentate interaction between Grignard reagents and bis[2-(N,N-dimethylamino)ethyl] ether moderates the reactivity of Grignard reagents, preventing the newly formed ketones from nuc...
متن کاملAromatic Iodides from Aromatic Organomercurials 13.2. Aromatic Bromides from Aromatic Organomercurials 13.3. Aromatic Chlorides from Aromatic Organomercurials 13.4. Aromatic Fluorides from Aromatic Organomercurials 13.5. Aromatic Nitriles from Aromatic Organomercurials 14. Improved Syntheses of Some Diaryliodonium Salts from Symmetric Diarylmercurials
This review reports some novel (or improved) synthetic methods for preparing a number of aromatic (carbocyclic and predominantly heterocyclic) organomercurials, particularly those derived from theophylline, theobromine and uracil, as well as some novel haloand cyano-demercuration reactions. We have also synthesized the first stable organic derivative of mercury(I), viz. 1,8-bis(acetoxydimercuri...
متن کاملTrialkylamine-mediated intramolecular acylation of alkenes with carboxylic acid chlorides.
Trialkylamine-mediated intramolecular cyclization of pent-4-enoyl chlorides was studied. Substitution with a tertiary alkyl group at the 2-position gave cyclopent-2-en-1-ones, while substitution with an aromatic group gave enol esters, which were formed by O-acylation of initially formed 3-chlorocyclopentanones with ketenes.
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ژورنال
عنوان ژورنال: Kobunshi
سال: 1974
ISSN: 0454-1138,2185-9825
DOI: 10.1295/kobunshi.23.389