Results 11 to 20 of about 6,084 (222)
Claisen Rearrangement Toward Cyclic Compound on Different Organic Synthesis Methods: Short Review
The synthesis of functional and complex organic compounds is majorly performed by the Claisen rearrangement method. Claisen rearrangement is one of [3,3] sigmatropic rearrangements, a complex method in the synthesis of organic compounds, where it is ...
Rizki Rachmad Saputra+7 more
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Novel Vulgarin Derivatives: Chemical Transformation, In Silico and In Vitro Studies
Vulgarin, an eudesmanolide sesquiterpene isolated from Artemisia judaica, was refluxed with iodine to produce two derivatives (1 and 2), which were purified and spectroscopically identified as naproxen methyl ester analogs.
Hanan G. Sary+2 more
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The molecular mechanisms of three intramolecular rearrangements (I, the rearrangement of allyloxycycloheptatriene to yield tricyclic ketones; II, the cycloaddition of a nitrone-alkene to render two tricyclic isoxazolidines; and III, the decomposition of ...
Abel Idrice Adjieufack+3 more
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A General and Scalable Synthesis of Polysubstituted Indoles
A consecutive 2-step synthesis of N-unprotected polysubstituted indoles bearing an electron-withdrawing group at the C-3 position from readily available nitroarenes is reported.
David Tejedor+2 more
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A series of novel 4-(aryl)-benzo[4,5]imidazo[1,2-a]pyrimidine-3-carbonitriles were obtained through the Povarov (aza-Diels–Alder) and oxidation reactions, starting from benzimidazole-2-arylimines.
Victor V. Fedotov+11 more
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An efficient metal-free domino reaction leading to structural/electronically divergent 1,2-dihydropyridines from easily accessible propargyl vinyl anilines via N-phenyl 3-aza-Cope sigmatropic rearrangement is reported with good to excellent yields using ...
Osamah Alduhaish+6 more
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Claisen, Cope and Related Rearrangements in the Synthesis of Flavour and Fragrance Compounds
A review of the use of the Claisen, Cope and related [3,3]-sigmatropic rearrangements, sequential ("tandem") sigmatropic rearrangements and the "ene" reaction in the syntheses of flavour and fragrance compounds is presented.
Janusz Nowicki
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Possibility of [1,5] sigmatropic shifts in bicyclo[4.2.0]octa-2,4-dienes [PDF]
The thermal equilibration of the methyl esters of endiandric acids D and E was subject to a computational study. An electrocyclic pathway via an electrocyclic ring opening followed by a ring flip and a subsequent electrocyclization proposed by Nicolaou ...
Catak, Saron+7 more
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Recent advances in the total synthesis of agelastatins [PDF]
Agelastatins represent an important family of marine alkaloids in terms of both exceptional biological activity and intriguing chemical structure.
Dong, Guangbin
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The paper describes a convenient and efficient method for regioselective synthesis of phosphorylated α-hydroxyallenes using an atom economical [2,3]-sigmatropic rearrangement of intermediate propargyl phosphites or phosphinites.
Ismail E. Ismailov+2 more
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