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New Cycloadditions in Synthesis

New Cycloadditions in Synthesis
合成中的新环加成
批准号:
7210383
负责人:
MARC L SNAPPER
金额:
$8.11万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2007-03-31

项目摘要

项目成果

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中文摘要
翻译
说明:(由申请人提供)介绍独特的化学物质
英文摘要
DESCRIPTION: (provided by applicant) The introduction of unique chemical transformations can considerably shorten synthetic pathways toward medicinally important compounds. Cycloadditions are known to be especially powerful reactions for building molecules of high complexity. The objectives of this proposal are to develop and use new cycloadditions of cyclobutadiene. It will be shown that highly functionalized cyclobutenes generated through intramolecular cyclobutadiene cycloadditions can provide a versatile platform for rapid entry into complex molecular systems. In particular, when used with other key transformations, the molecular complexity and structural strain of the cycloadducts offer unique opportunities for the efficient construction of medium ring-containing natural products with intriguing biological activities. The cyclobutene cycloadducts will be used in the preparation of cycloheptanoid and cyclooctanoidcontaining products. Inter- and intramolecular cyclopropanations of the cyclobutenes, followed by selective carbon-carbon bond fragmentations, will be used to generate effectively the 5-7 ring system found in numerous biologically active natural products. Similarly, a (2+2) photocyclization/fragmentaton strategy will provide access to the 5-8-5 ring system. Concise applications of the chemistry toward the synthesis of diterpenes, such as kalmanol, are detailed. In short, the combination of developing new routes toward cyclobutadiene complexes, investigating novel cycloadditions of these complexes, and demonstrating the utility of the cycloadducts in medium ring synthesis will offer improved opportunities for building molecules of biological significance.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
Intramolecular cyclobutadiene cycloaddition/cyclopropanation/thermal rearrangement: an effective strategy for the asymmetric syntheses of pleocarpenene and pleocarpenone.
分子内环丁二烯环加成/环丙烷化/热重排:多卡尔烯和多卡尔烯酮不对称合成的有效策略。
DOI: 10.1021/ja0674340
发表时间: 2007
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Williams,MichaelJ, Deak,HollyL, Snapper,MarcL]
通讯作者: Snapper,MarcL
Solvent-controlled intramolecular [2 + 2] photocycloadditions of alpha-substituted enones.
α-取代烯酮的溶剂控制分子内 [2 2] 光环加成。
DOI: 10.1021/ja060968g
发表时间: 2006
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Ng,StephanieM, Bader,ScottJ, Snapper,MarcL]
通讯作者: Snapper,MarcL
DOI: 10.1021/ja0203162
发表时间: 2002-11
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [J. Limanto;John A. Tallarico;James R. Porter;Kelli S. Khuong;K. Houk;M. Snapper]
通讯作者: J. Limanto;John A. Tallarico;James R. Porter;Kelli S. Khuong;K. Houk;M. Snapper
Lewis acid-mediated generation of bicyclo[5.3.0]decanes and bicyclo[4.3.0]nonanes.
路易斯酸介导生成双环[5.3.0]癸烷和双环[4.3.0]壬烷。
DOI: 10.1021/ol051498i
发表时间: 2005
期刊: Organic letters
影响因子: 5.2
作者: [Deak,HollyL, Williams,MichaelJ, Snapper,MarcL]
通讯作者: Snapper,MarcL
New Cycloadditions in Synthesis
  • 批准号:
    7093948
  • 项目类别:
  • 资助金额:
    $6.56万
  • 财政年份:
    2002
  • 负责人:
    MARC L SNAPPER
  • 依托单位:
New Cycloadditions in Synthesis
  • 批准号:
    6430639
  • 项目类别:
  • 资助金额:
    $25.99万
  • 财政年份:
    2002
  • 负责人:
    MARC L SNAPPER
  • 依托单位:
New Cycloadditions in Synthesis
  • 批准号:
    6881192
  • 项目类别:
  • 资助金额:
    $23.61万
  • 财政年份:
    2002
  • 负责人:
    MARC L SNAPPER
  • 依托单位:
New Cycloadditions in Synthesis
  • 批准号:
    6732728
  • 项目类别:
  • 资助金额:
    $23.61万
  • 财政年份:
    2002
  • 负责人:
    MARC L SNAPPER
  • 依托单位:
海外基金