New Methods for the Concise Synthesis of Bioactive Polycyclic Molecules
New Methods for the Concise Synthesis of Bioactive Polycyclic Molecules
批准号:
8266433
负责人:
Regan James Thomson
金额:
$27.93万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-01 至 2014-05-31
关键词:
AreaBiologicalBiological FactorsChemical StructureChemicalsChemistryClinicalComplexCouplingCyclohexanonesDataDevelopmentDimerizationDiseaseEnsureEquilibriumEthersFuransGenerationsGoalsHealthHumanImmunomodulatorsKetonesMalignant NeoplasmsMediatingMedicineMethodologyMethodsOutcomeOutcomes ResearchPathway interactionsPreparationProceduresProcessPropertyPyrrolesReactionResearchSchemeSilanesSiliconSolutionsStructureSynthesis ChemistryTherapeuticanticancer activitybasecatalystclinically relevantcombatdiketonedrug candidateenolenolatehuman diseaseinnovationlomaiviticin Ametacycloprodigiosinnovel strategiesnovel therapeuticsoxidationsilanesmall molecule librariestechnique developmenttherapeutic development
中文摘要
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英文摘要
PROJECT SUMMARY/ABSTRACT
The discovery and development of effective chemical therapeutics for human disease is
limited by the shortcomings of synthetic chemistry that make investigating important chemical
structures difficult. In particular, the clinical potential of many complex polycyclic structures is
under-explored due to a lack of methods for their preparation. Bridging this gap will allow many
new structures to be synthesized rapidly, leading to an increased rate at which new therapeutics
are discovered.
Our long-term goal is to make significant contributions to both chemistry and medicine
by developing general synthetic methods to construct biologically active complex polycyclic
structures. The overall objective of our current research is to develop the oxidative coupling of
silicon-tethered enolates as a powerful method to prepare complex structures that contain
contiguous stereocenters. The paucity of available methods limits the use of such structures in
chemical library synthesis and makes the efficient preparation of clinically relevant natural
products difficult. Our rationale for investigating silyl bis-enol ethers is that they can mediate the
coupling of two different chemical fragments and simultaneously control the stereochemical
outcome of bond formation, thereby affording concise syntheses of complex structures.
The Specific Aims of this proposal are: 1. Develop and utilize silyl bis-enol ether-based
oxidation as a powerful new method to construct contiguous stereocenters; 2. Develop
multicomponent coupling processes for rapid generation of complex bioactive molecules; and 3.
Develop new oxidative bond-forming reactions that extend beyond enol-enol coupling.
This proposed research is innovative because the silicon-tether acts to control both
heterocoupling vs. homocoupling, and stereoselectivity for oxidative enolate bond formation.
The development of techniques for fashioning quaternary stereocenters, vicinal stereoarrays,
and tandem multicomponent coupling sequences will generate complexity efficiently. Additional
research into Lewis base activation will provide enantioselective methods for preparing these
structures. The invention of new oxidative bond-forming reactions will expand the usefulness of
the silicon-tether concept to a wealth of challenging compounds. The expected outcomes of this
research will be the concise synthesis of many medicinally important structures that are of
significant challenge to current methods. This proposed research is significant for human health
because it is expected to provide complex polycyclic structures in quantities that will ensure
their utilization in discovering new chemical therapeutics.
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New Methods for the Concise Synthesis of Bioactive Polycyclic Molecules
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批准号:8072644
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项目类别:
-
资助金额:$27.98万
-
财政年份:2009
-
负责人:Regan James Thomson
-
依托单位:
New Methods for the Concise Synthesis of Bioactive Polycyclic Molecules
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批准号:7843702
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项目类别:
-
资助金额:$28.32万
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财政年份:2009
-
负责人:Regan James Thomson
-
依托单位:
New Methods for the Concise Synthesis of Bioactive Polycyclic Molecules
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批准号:8474634
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项目类别:
-
资助金额:$26.89万
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财政年份:2009
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负责人:Regan James Thomson
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依托单位:
海外基金