CAS: 167171-03-1; (R)-2-(2-(Diphenylphosphino)Phenyl)-4-Phenyl-4,5-Dihydrooxazole

该化合物是一种有机氧化氮衍生物,具有二苯基磷替代成分,增强了其在非对称催化解和协调化学中的效用.(4R)配置确保了合成应用中的对应选择性性性能,特别是在过渡性金属催化反应中.其硬性氧化氮脊椎和磷碱混合物有助于稳定性和效率,使其对形成具有高度立体控制的金属综合体很有价值.该化合物非常适合交叉相撞,氢化和其他立体变异,对反应结果提供精确的控制.其结构特征还促进了工业过程中的可再循环性和减少催化剂负荷.

结构式图片

上下游产品

diphenylphosphane (4R)-2-(2-fluorophenyl)-4-phenyl-4,5-dihydro-1,3-oxazole potassium diphenylphosphine D-2-phenylglycinol

合成工艺路线路线简述

    L-苯甘氨酸置于copper(L) Iodide,Lithium Aluminium Tetrahydride,氯苯,Zinc(II) Chloride体系中,用 四氢呋喃,甲苯 用作溶剂,化学反应 6.34H,反应生成(R)-(-)-2-[2-(二苯基膦)苯基]-4-苯基-2-噁唑啉
    参考文献:铜(i)膦恶唑啉配合物:配体取代和立体需求对电化学和光物理性质的影响.
    标题:铜(i)膦恶唑啉配合物:配体取代和立体需求对电化学和光物理性质的影响.
    摘要:合成了七个基于异双峰p ^ N配体的纯铜cui复合物,并对其进行了全面的表征.为了研究结构-性质之间的关系,系统地改变了膦恶唑啉(phox)配体上取代基的类型,大小,数量和构型.为此,X射线衍射,NMR光谱,稳态吸收和发射光谱,时间分辨发射光谱,猝灭实验和循环伏安法的组合被用于评估光物理和电化学性质.此外,基于时间的密度泛函理论计算也被用来分析激发态的结构和特性.令人惊讶的是,发现对各个p ^ N配体的手性有很强的依赖性,而不同取代基的具体种类和大小对溶液的性质影响很小.最重要的是,除c3以外的所有配合物在溶液中都是光稳定的,并显示出完全可逆的氧化还原过程.牺牲性还原剂被施加以证明在光照射下成功的电子转移.这些特性使这类光敏剂成为太阳能转化问题的潜在候选者.
    Doi:10.1002/chem.201904379

    海关参考信息

    专利信息


    专利号:US-9518034-B2
    优先权日:2013-10-14
    标题 :Synthesis of chiral enaminones, their derivatives, and bioactivity studies thereof
    发明人:STOLTZ BRIAN M; DOUGHERTY DENNIS A; DUQUETTE DOUGLAS; DUFFY NOAH
    权利人:CALIFORNIA INST OF TECHN
    摘要:This invention provides enantioenriched heterocyclic enaminone compounds with quaternary stereogenic centers and novel methods of preparing the compounds. Methods include the method for the preparation of a compound of formula (I): n ncomprising treating a compound of formula (II):n n nwith a transition metal catalyst under alkylation conditions.

    专利号:US-11377396-B2
    优先权日:2014-12-18
    标题 :Enantioselective synthesis of α-quaternary Mannich adducts by palladium-catalyzed allylic alkylation
    发明人:STOLTZ BRIAN M; NUMAJIRI YOSHITAKA; PRITCHETT BEAU P; CHIYODA KOJI
    权利人:CALIFORNIA INST OF TECHN
    摘要:This invention provides enantioenriched Mannich adducts with quaternary stereogenic centers and novel methods of preparing the compounds. Methods include the method for the preparation of a compound of formula (I): n ncomprising treating a compound of formula (II):n n nwith a transition metal catalyst under alkylation conditions.

    专利号:US-2016096810-A1
    优先权日:2014-10-07
    标 题 :Enantioselective synthesis of dialkylated n,o-heterocycles by palladium-catalyzed allylic alkylation
    发明人:STOLTZ BRIAN M; NUMAJIRI YOSHITAKA; BEHENNA DOUGLAS C
    权利人:STOLTZ BRIAN M; NUMAJIRI YOSHITAKA; BEHENNA DOUGLAS C
    摘要:This invention provides enantioenriched N,O-heterocyclic compounds with quaternary stereogenic centers and novel methods of preparing the compounds. Methods include the method for the preparation of a compound of formula (I): n n n n n n n n n n comprising treating a compound of formula (II): n n n n n n n n n n with a transition metal catalyst under alkylation conditions.

    专利号:US-2020157020-A1
    优先权日:2014-12-18
    标题:Enantioselective synthesis of alpha-quaternary mannich adducts by palladium-catalyzed allylic alkylation

    专利号:US-2015105552-A1
    优先权日:2013-10-14
    标 题 :Synthesis of chiral enaminones, their derivatives, and bioactivity studies thereof

    专利号:US-2016176773-A1
    优先权日:2014-12-18
    标 题 :ENANTIOSELECTIVE SYNTHESIS OF alpha-QUATERNARY MANNICH ADDUCTS BY PALLADIUM-CATALYZED ALLYLIC ALKYLATION
    安徽凯泰莱铂科技有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.krl-tech.com
    企业联系电话:0512-66834346👤
    📞安徽凯泰莱铂科技有限公司 ⚠️参考联系方式
    联系人:郑朝晖
    电话:0512-66834346
    手机:17751128648

    邮箱:13916109676@163.com
    通信地址: 合肥市高新区孔雀台路习友路口国家健康大数据产业园C2-01栋
    邮编: 230041
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:合肥市高新区孔雀台路习友路口国家健康大数据产业园C2-01栋
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Catalytic Enantioselective Synthesis Of Cyclobutenes From Alkynes And Alkenyl Derivatives
    作者:Mahesh M. Parsutkar,Vinayak Vishnu Pagar,T. V. Rajanbabu |发布日期:2019.9.25
    摘要:Compounds From Readily Available Precursors, Using Scalable And Environmentally Benign Chemistry, Can Greatly Impact Their Design, Synthesis And Eventually Manufacture On Scale. Functionalized Cyclobutanes And Cyclobutenes Are Important Structural Motifs Seen In Many Bioactive Natural Products And Pharmaceutically Relevant Small Molecules. They Are Also Useful Precursors For Other Classes Of Organic Compounds

    合成参考文献


    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 208.
    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 202.
    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 213.
    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 154.
    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 211.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知