Selective C-H Bond Functionalization in Complex Organic Synthesis
Selective C-H Bond Functionalization in Complex Organic Synthesis
批准号:
7374075
负责人:
DALIBOR SAMES
金额:
$31.1万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-03-01 至 2011-08-31
关键词:
AchievementAcidsAlkenesAlkylationAminesAreaAzolesBiologicalBiological FactorsBiological SciencesChemicalsClassComplexCouplingCyclizationDevelopmentEstersFelis catusFundingFutureHealthHeterocyclic CompoundsLaboratoriesLigandsMedicineMethodsMolecularNew AgentsObject AttachmentOrganic SynthesisPharmacologic SubstancePreparationProcessProgress ReportsProteinsRangeRateReactionResearchSeriesShapesTransition Elementsbasedesigndesirehuman diseaseinterestnovel strategiesprogramstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This program focuses on the development of new catalytic methods for selective functionalization of C-H bonds in complex organic substrates of biological interest. The ability to transform selectively a preset C-H bond to a new C-C bond carries significant consequences for the practice of organic synthesis. The previous funding period established a vital and productive research program. In the process, we demonstrated that selective C-H bond activation and functionalization can be achieved in complex organic substrates and that these processes can be made catalytic in the transition metal. Also, our research showed that C-H bond transformations offer exciting strategic opportunities in synthesis. The next funding period will continue these efforts with particular emphasis on the development of new C-H to C-C transformations in the context of heterocyclic compounds (both saturated heterocycles and heteroarenes). Heterocycles are indispensable structural units frequently found in biologically active compounds, including natural products, protein ligands, and pharmaceuticals. New synthetic methods in this area are of high importance to life sciences, medicine, and health. New chemical transformations not only facilitate access to desired compounds of biological and medicinal interest, but also shape the very process of molecular design. In specific terms, the future projects include C-H arylation of saturated heterocycles (1-arylation of amines equipped with a new directing group; sp3 C-H bonds), direct C-H arylation of complex azole heteroarenes (sp2 C-H bonds). Also, two new approaches to cross-coupling of sp3 C-H bonds and alkenes (1-alkylation of saturated heterocycles) will be pursued: first, the intermolecular transition metal-catalyzed alkylation; and second, Lewis acid catalyzed intramolecular cyclization. These new methods will not only impact the synthesis of specific target molecules, but also will reshape the synthetic strategies for preparation of series of compounds. Selective C-H Bond Functionalization in Complex Organic Synthesis Resubmission Renewal Application, GM 60326
New methods for the preparation of research probes, medicinal agents, and new pharmaceuticals will be developed. Such research tools will increase the rate of understanding and potential treatment of human diseases.
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