Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles

Herein we report an approach to the formation of 5-alkynyl-1,3-dioxin-4-ones using Suzuki-Miyaura cross-coupling reaction of potassium alkynyltrifluoroborate salts with 2,2,6-trimethy1-5-iodo-1,3-dioxin-4-one. The resulting 5-ethynyltrimethylsilyl-1,3-dioxin-4-ones obtained through the Sonogashira reaction were further reacted in a Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition to form functionalized 1,4-disubstituted-1,2,3-triazoles in good yields, using mild conditions and ultrasonic radiation to expedite the reaction. (C) 2011 Elsevier Ltd. All rights reserved.

1.° Chronica de narratione inchoationis et promotionis ordinis Cartusiensis. — 2.° Chronica de exordio ordinis Cartusiensis. — 3.° Bernardus de contemplatione. — 4.° Responsiones cujusdam Prioris majoris Cartusiae ad quemdam Monachum ejusdem ordinis Cartusiensis, Bonifacium nomine. — 5.° Miraculum de sancto Mauricio et Udone, Episcopo, editum anno 955. — 6.° Nonnulla ad vitam sancti Ludovici, Regis Francorum, spectantia. — 7.° Tractatus de approbatione et confirmatione ordinis Cartusiensis à sancta Romana Ecclesia : ad calcem subjicitur epistola concilii Basileensis ad Cartusienses. — 8.° Practica, quomodo procedi solet in electione Priorum ordinis Cartusiensis.

Colbertinus

1.° Sextus Pompeius Festus de verborum significatione. — 2.° Anonymi tractatus de rhetorica et de dialectica. — 3.° Aristotelis epistola ad Alexandrum de secretis secretorum. — 4.° Senecae liber ad Galeotum de vita beata. — 5.° Oeconomicorum Aristotelis liber : interprete Leonardo Aretino. — 6.° Isidori, Hispalensis, synonyma. — 7.° Messalae Corvini ad Octavium Augustum de progenie sua breve compendium.

Colbertinus

1.° Codicis Theodosiani libri sexdecim ; hîc solae occurrunt interpretationes : praemittitur opusculum quod inscribitur ; Judicia Dei. — 2.° Theodosii Junioris, Valentiniani III. Marciani et Majoriani novellae constitutiones. — 3.° Gaii Institutionum epitome. — 4.° Julii Pauli sententiarum libri quinque, cum interpretationibus. — 5.° Excerpta e Codice Gregoriano, Hermogeniano et Papianeo. — 6.° Leges divi Anthemii. — 7.° Alia excerpta ex Codice Gregoriano

Colbertinus, antea Jacobi Augusti Thuani

1.° Liber inscriptus : Cautelae Bagaroti, juris Professoris. — 2.° Anonymi tractatus de causarum exercitiis. — 3.° Summula de libellis : authore Bernardo Dorna, Provinciali. — 4.° Cavillationes domini Uberti de Bobio. — 5.° Distinctiones a domino Ugone compositae, et a domino Alberico consummatae. — 6.° Summa de arbitris a domino B. promulgata, missa ad A. F. Romanae Ecclesiae Cancellarium. — 7.° Opusculum, cujus titulus est : Arbor actionum. — 8.° Anonymi tractatus de actionibus. — 9.° Formularium procurationum, secundum usum curiae Romanae

Colbertinus

The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

Preludeja op. 17 nrot 2, 6, 9, 10, 11, 12, 15 & 23

Digitoitu 13. 8. 2008.