CAS: 13511-38-1; 3-Chloro-2,2-Dimethylpropanoic Acid

相似化合物

13401-56-4 17831-70-8 106315-37-1

上下游产品

1,4-dichloro-3,3-dimethyl-butan-2-one Trimethylacetic acid 3-Chloro-2-methylpropene chlorine methyl 3-chloro-2,2-dimethylpropionate O-benzyl-β-chloropivalohydroxamic acid 3-Chloropivaloyl chloride 2,2-dimethyl-3-(phenylthio)propionic acid

N-[2,2-Dimethylpropanoyl]-S-Methyl-S-2-Pyridylsulfoximine置于n-氯代酞酰亚胺,水,氢溴酸,Palladium Diacetate,溶剂黄146体系中,用 1,2-二氯乙烷 用作溶剂,化学反应 28.0H,反应生成3-氯-2,2-二甲基丙酸
参考文献:磺胺嘧啶辅助的pd(II)催化的初级β-C(sp 3)-H键的溴化和氯化反应
标题:磺胺嘧啶辅助的pd(II)催化的初级β-C(sp 3)-H键的溴化和氯化反应
摘要:在n-Br / Cl的影响下,实现了mpys-N-酰胺的1°-β-C(sp 3)-H键的s-甲基-S-2-吡啶基亚磺酰亚胺(mpys)定向溴化和氯化.-邻苯二甲酰亚胺和pd(II)催化剂.α-二甲基mpys-N-酰胺的顺序卤化和乙酰氧基化可构建高度官能化的α-三取代脂族酸衍生物.从卤化产物中裂解出mpys指导基团并回收.
Doi:10.1021/ol502337B

专利信息

专利号:US-7355036-B2
优先权日:2001-07-03
标 题 :Two-stage protective groups for the synthesis of biopolymers
发明人：GUEIMIL RAMON; SCHEFFLER MATTHIAS; STAEHLER PEER F; BEIJER BARBRO
权利人:FEBIT AG
摘要:The invention relates to a method for the synthesis of a nucleic acid by gradual breakdown from protected synthesis building blocks carrying two-stage protective groups. The two-stage protective groups are split by means of a first exposure step and a subsequent chemical treatment step

专利号:US-9359376-B2
优先权日:2011-04-08
标题:Substituted methylformyl reagents and method of using same to modify physicochemical and/or pharmacokinetic properties of compounds
发明人：DUGAR SUNDEEP; MAHAJAN DINESH; HOLLINGER FRANK PETER
权利人:DUGAR SUNDEEP; MAHAJAN DINESH; HOLLINGER FRANK PETER; SPHAERA PHARMA PTE LTD
摘要:The present invention relates to the synthesis and application of novel chiral/achiral substituted methyl formyl reagents to modify pharmaceutical agents and/or biologically active substances to modify the physicochemical, biological and/or pharmacokinetic properties of the resulting compounds from the unmodified original agent.

专利号:US-2007275908-A1
优先权日:2003-03-06
标 题:Methods and Compositions for the Enzymatic Synthesis of Gangliosides

专利号:US-4742052-A
优先权日:1981-07-15
标题:Antibacterial β-lactam compounds
发明人：SUNAGAWA MAKOTO; MATSUMURA HARUKI; INOUE TAKAAKI; ENOMOTO MASAO
权利人:SUMITOMO PHARMA
摘要:Novel beta -lactam compounds classified into penem compounds, a process for preparing the same and use of such beta -lactam compounds are disclosed. These beta -lactam compounds exhibit excellent antimicrobial activities useful as pharmaceuticals or they are important intermediates for the synthesis of compounds having antimicrobial activities.

专利号:EP-1603932-B1
优先权日:2003-03-06
标题:Methods and compositions for the enzymatic synthesis of gangliosides

专利号:WO-2004080960-A2
优先权日:2003-03-06
标题 :Methods and compositions for the enzymatic synthesis of gangliosides