CAS: 131833-93-7; (4S,4'S)-2,2'-(Propane-2,2-Diyl)Bis(4-(Tert-Butyl)-4,5-Dihydrooxazole)

该化合物是用于非对称合成和催化的显赫性复合物.该物质具有中丙烷脊柱,有两个氧气环,由五人组成,含有氮和氧的异丙环.三丁基组的存在增强了其成份,有助于其作为协调化学的一流体的功效.辛辛醇-辛醇-丁基-1,3-氧基-辛醇基]正丙烷在推动特定反应途径和增强化学选择性方面所发挥的作用得到承认.一般而言,它表现出有机溶剂的溶性,有助于其在各种化学工艺中的应用.此外,其结构特性使其能够与过渡金属形成稳定的复合体,进一步扩大其在催化中的用途.

结构式图片

欧盟法规

C&L通报

上下游产品

2,2-dimethylmalononitrile (S)-tert-leucinol (S,S)-2,2'-methylenebis(4-tert-butyl-2-oxazoline) methyl iodide

合成工艺路线路线简述

  • 合成目标产物 (S,S)-(-)-2,2'-Isopropylidenebis(4-Tert-Butyl-2-Oxazoline) 主要起始原料 Dimethylmalonic Acid
  • (文献来源)合成步骤主要原料 Dimethylmalonic Acid
📜二甲基丙二酸置于草酰氯,三乙胺,N,N-二甲基甲酰胺体系中,用 二氯甲烷 用作溶剂,化学反应 51.5H,反应生成(S,S)-(-)-2,2'-异亚丙基双(4-叔丁基-2-恶唑啉)
参考文献:Lewis Acid Catalysed Asymmetric One-Carbon Ring-Expansion Of Prochiral Cyclobutanones
标题:Lewis Acid Catalysed Asymmetric One-Carbon Ring-Expansion Of Prochiral Cyclobutanones
摘要:摘要:本文描述了手性β-取代环戊酮的亲核亚甲基插入反应,提供了在合成和天然产物中作为重要结构基元的手性β-取代环戊烯酮的访问途径.商业上可获得的三甲基硅基以及其他硅基重氮甲烷作为一碳合成物,而三氟甲基硫酸钪则被发现是一种有效的路易斯酸催化剂.通过使用双噁唑啉配体,实现了对许多β-取代环戊烯酮的对映诱导,包括带有全碳季节立体中心的例子.
Doi:10.1055/s-0042-1751386

海关参考信息

专利信息


专利号:US-7186709-B2
优先权日:2002-08-27
标 题:Dihydropyrancarboxamides and uses thereof
发明人:SCHREIBER STUART L; STAVENGER ROBERT A; MITCHISON TIMOTHY J; MALIGA ZOLTAN
权利人:HARVARD COLLEGE
摘要:The present invention provides novel dihydropyrancarboxamide compounds of formula (I): n nand collections of these compounds, and provides methods for the synthesis of these compounds; wherein R 1 –R 6 are as defined herein. Additionally, the present invention provides pharmaceutical compositions and methods for treating disorders such as proliferative diseases, and cancer, to name a few.

专利号:US-8633182-B2
优先权日:2012-05-30
标题:Indanyloxyphenylcyclopropanecarboxylic acids
发明人:HAMPRECHT DIETER; FRATTINI SARA; LINGARD IAIN; PETERS STEFAN
权利人:HAMPRECHT DIETER; FRATTINI SARA; LINGARD IAIN; PETERS STEFAN; BOEHRINGER INGELHEIM INT
摘要:The present invention relates to compounds of general formula I, n nwherein the groups R 1 , R 2 , R 3 , m and n are defined as in claim 1 , which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2. Furthermore, the invention relates to novel intermediates, useful for the synthesis of compounds of formula I.

专利号:CN-115304568-A
优先权日:2022-05-17
标 题 :Asymmetric synthesis of 6-azidomethylene-1-aryl-3-oxabicyclo[3,1,0]hexan-2-ones

专利号:CN-114031573-A
优先权日:2022-01-10
标 题:Method for recovering ligands in asymmetric synthesis of S-(+)-2,2-dimethylcyclopropanecarboxylic acid

专利号:CN-107903276-A
优先权日:2017-11-17
标题 :A kind of asymmetric synthesis method of ring E of harringtonine skeleton

专利号:CN-107903276-B
优先权日:2017-11-17
标 题 :A kind of asymmetric synthesis method of ring E of harringtonine skeleton

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

合成参考文献


摘要:Okamoto, K.; Ohe, K., Science of Synthesis Knowledge Updates, (2020) 1, 98.
摘要:Kizirian, J.-C., Science of Synthesis Knowledge Updates, (2012) 2, 109.
摘要:Muchalski, H.; Johnston, J. N., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 161.
摘要:Hata, S.; Sibi, M. P., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 896.
摘要:Hata, S.; Sibi, M. P., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 913.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知