0000000000555502

AUTHOR

Julien Letessier

showing 3 related works from this author

Synthesis of a Naphtho-pyrido-Annulated Iodonium Salt and Pd-Catalyzed Transformation to 7H-Naphtho[1,8-bc][1,5]naphthyridine

2013

Nitropyridylnaphthalene is the central intermediate for the synthesis of naphthonaphthyridine and benzo-δ-carboline. Whereas the Cadogan reaction gives the carboline, transformation of the nitro group to iodo followed by oxidation and cyclization results in an iodonium salt. A twofold Pd-catalyzed amination leads to the naphthyridine.

chemistry.chemical_classificationTransformation (genetics)ChemistryOrganic ChemistryNitroSalt (chemistry)chemistry.chemical_elementIodineMedicinal chemistryCatalysisAminationCatalysisPalladiumSynthesis
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ChemInform Abstract: Synthesis of a Naphtho-pyrido-Annulated Iodonium Salt and Pd-Catalyzed Transformation to 7H-Naphtho[1,8-bc][1,5]naphthyridine.

2014

Nitropyridylnaphthalene is the central intermediate for the synthesis of naphthonaphthyridine and benzo-δ-carboline. Whereas the Cadogan reaction gives the carboline, transformation of the nitro group to iodo followed by oxidation and cyclization results in an iodonium salt. A twofold Pd-catalyzed amination leads to the naphthyridine.

chemistry.chemical_classificationTransformation (genetics)ChemistryNitroOrganic chemistrySalt (chemistry)General MedicineAminationCatalysisChemInform
researchProduct

ChemInform Abstract: Microwave-Assisted Synthesis of 1,3-Disubstituted β-Carbolines from α-(Alkylideneamino)nitriles and Gramine.

2012

The title reaction produces indole derivatives of type (V) whose cyclization leads to formation of the desired alkaloid skeletons.

Indole testGraminechemistry.chemical_compoundChemistryAlkaloidOrganic chemistryGeneral MedicineMicrowave assistedChemInform
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