CAS: 77877-20-4; (4R,5S)-4-Methyl-5-Phenyl-3-Propionyloxazolidin-2-One

该化合物是非对称合成中广泛使用的一种手性氧化氮基酮辅助剂,其硬性双环结构和定义明确的立体化学能够进行高度对应的选择性变异,特别是在埃文斯型藻类和藻类反应中.4-甲基和5苯基替代成分加强了...

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CAS号77943-39-6 (4R,5S)-(+)-4-甲... | CAS号79-03-8 丙酰氯 | CAS号123-62-6 丙酸酐 | CAS号40626-29-7 右旋盐酸去甲麻黄碱 | CAS号492-39-7 Cathine | CAS号37577-28-9 左旋去甲麻黄碱 | CAS号598-26-5 二甲基乙烯酮 | CAS号24423-87-8 2-oxido-3,4-dih... | CAS号77943-39-6 (4R,5S)-(+)-4-甲... | CAS号16251-45-9 (4S,5R)-(-)-4-甲...

合成工艺路线路线简述

    📜去甲伪麻黄碱置于正丁基锂,Potassium Carbonate体系中,用 甲苯 作为反应溶剂,化学反应 2.0H,反应生成 (4R,5S)-3-丙酰基-4-甲基-5-苯基-2-噁唑烷酮
    参考文献:Brimble,Margaret A.,Australian Journal Of Chemistry,1990,Vol. 43,# 6,P. 1035-1046
    标题:Brimble,Margaret A.,Australian Journal Of Chemistry,1990,Vol. 43,# 6,P. 1035-1046

    海关参考信息

    专利信息


    专利号:US-6603015-B2
    优先权日:1999-03-29
    标题:Synthesis of epothilones
    发明人:GEORG GUNDA I; NAIR SAJIV K; REIFF EMILY; TUNOORI ASHOK RAO
    权利人:UNIV KANSAS
    摘要:Commercially feasible methods for synthesizing various epothilones precursors needed for the preparation of final epothilones are provided, including techniques for the synthesis of epothilone segment A and C precursors. Segment C precursors are prepared using starting nitriles, which can alternately be oxidized to ketones and converted, or reacted to form the diol with subsequent conversion to the segment. Segment A precursors are prepared by reacting a starting enone with a chiral catalyst to give an intermediate alcohol in high enantomeric excess, followed by conversion of the alcohol to the desired Segment A precursor.

    专利号:US-7700783-B2
    优先权日:2003-10-09
    标题 :Synthesis of discodermolide and variants thereof
    发明人:SMITH III AMOS B; FREEZE BRIAN SCOTT; XIAN MING
    权利人:UNIV PENNSYLVANIA
    摘要:Processes for synthesizing a compound of Formula (I) are provided by reacting a compound of Formula (i) with a compound of Formula (xx).

    专利号:US-6457303-B1
    优先权日:1999-03-29
    标题:Synthesis of epothilones
    发明人:GEORG GUNDA I; NAIR SAJIV K; REIFF EMILY; TUNOORI ASHOK RAO; HENRI JOHN T
    权利人:UNIV KANSAS
    摘要:Various epothilone precursors needed for the preparation of final epothilones are provided.

    专利号:EP-1058679-B1
    优先权日:1998-02-25
    标 题 :Synthesis of epothilones, intermediates thereto and analogues therof
    发明人:DANISHEFSKY SAMUEL J; BALOG AARON; BERTINATO PETER; SU DAI-SHI; CHOU TING-CHAU; MENG DONGFANG; KAMENECKA TED; SORENSEN ERIK J; KUDUK SCOTT; HARRIS CHRISTINA; ZHANG XIU-GUO; BERTINO JOSEPH R
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides convergent processes for preparing epothilone A and B, desoxyepothilones A and B, and analogues thereof, useful in the treatment of cancer and cancer which has developed a multidrug-resistant phenotype. Also provided are intermediates useful for preparing said epothilones.

    专利号:US-2002156289-A1
    优先权日:1999-03-29
    标 题 :Synthesis of epothilones

    专利号:US-2002165415-A1
    优先权日:1999-03-29
    标 题:Synthesis of epothilones

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    📌 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:Synthetic Studies In The Lysocellin Family Of Polyether Antibiotics. The Total Synthesis Of Ferensimycin B
    作者:David A. Evans,Richard P. Polniaszek,Keith M. Devries,Denise E. Guinn,David J. Mathre |发布日期:1991.9
    摘要:A Convergent Asymmetric Synthesis Of The Polyether Antibiotic Ferensimycin B Has Been Completed. Chiral Enolate Bond Constructions Were Employed To Establish Seven Of The 16 Stereocenters Of The Subunits 35 And 52, Which Comprise The C& And Ci&3 Portions Of Ferensimycin B. The Stereogenic Centers At C3, C4, Cg, Clo, Ci6, C,,, And Cis Were Incorporated Through Internal Asymmetric Induction, While Those

    合成参考文献


    摘要:Gennari, C.; Ceccarelli, S.; Piarulli, U., Science of Synthesis, (2005) 6, 367.
    摘要:Gennari, C.; Ceccarelli, S.; Piarulli, U., Science of Synthesis, (2005) 6, 393.
    摘要:Gennari, C.; Ceccarelli, S.; Piarulli, U., Science of Synthesis, (2005) 6, 380.
    摘要:Mahrwald, R.; Schetter, B., Science of Synthesis, (2008) 36, 860.
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