[2]李朝龙,魏彦君,王华.氨基保护的(R)-3-氨基哌啶的制备方法[P].上海市:CN201310048432.5,2016-09-14. [3]Kadyrov R ,Tok L O .Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane[J].Synthesis,2021,53(19):3573-3577. 免责申明...
Uses (R)-3-(Boc-amino)piperidine is used as an organic chemical synthesis intermediate. (R)-3-(Boc-Amino)piperidine Preparation Products And Raw materials Preparation Products (R)-3-Amino-1-methyl-piperidineTag:(R)-3-(Boc-Amino)piperidine(309956-78-3) Related Product Information ...
(S)-3-氨基-1-苄基哌啶 (S)-1-Benzylpiperidin-3-amine dihydrochloride CAS No.:307532-02-1 (R)-3-Boc-氨基哌啶 (R)-3-(Boc-Amino)piperidine CAS No.:309956-78-3 (R)-1-苄基-3-氨基哌啶二盐酸盐 (R)-1-Benzylpiperidin-3-amine dihydrochloride ...
本发明的(R)-3-氨基哌啶(I)的不对称合成方法工艺合理,路线简洁,利用手性诱导以较高的ee值得到了所要的产品,而且原料便宜,无需拆分,实现了无废弃异构体排放,适合于大规模工业化生产. (R) -3 present invention - amino-piperidine (I), asymmetric synthesis process is reasonable, simple route using chiral ...
英文名称3-Amino-1-Boc-piperidine 储存温度充氩 运输条件常规运输 产品介绍 Product Application: 3-Amino-1-Boc-piperidine is used as an organic chemical synthesis intermediate. 关联靶点(其它种属) 名称和识别符 数据库链接 化学和物理性质 安全和危险性(GHS) ...
2.3.3Alkylation reactions. Synthesis of asparagine analogs (17) and(18) Diastereoselective alkylation of (R)‐(+)‐camphor‐based glycylimine (19) with 3‐bromo‐2‐fluoropropene gave (R)‐(+)‐2‐amino‐4‐fluoropent‐4‐enoic acid with 38% overall yield and 90% ee after hydrolytic depro...
piperidinesasymmetric synthesisaddition reactionα-Amino-3-piperidinylphosphonates were conveniently prepared from 3-piperidinone, by nucleophilic addition of phosphite to the iminium ion formed by in situ condensation of this ketone with chiral benzylic amines. Subsequent deprotection of N-Boc group, ...
Highly Enantioselective Catalytic Dynamic Resolution of N-Boc-2-lithiopiperidine: Synthesis of (R)-(+)-N-Boc-Pipecolic Acid, (S)-()-Coniine, (S)-(+)-Pellet... Highly enantioselective catalytic dynamic resolution of N-Boc-2-lithiopiperidine: synthesis of (R)-(+)-N-Boc-pipecolic acid, ...
ChemInform Abstract: Synthesis of (2S*,4R*,5S*)‐Piperidinetricarboxylic Acid, a Non‐Proteinogenic Amino Acid Isolated from Clitocybe Acromelalgaamino acids, peptidesChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading ...
3-methylaminopiperidine, an intermediate for the manufacturing of Balofloxacin, was synthesis from nicotinic amide in four steps. 研究了烟酰胺的Hofmann降解、甲酰化、一次还原及二次还原,旨在研究出巴洛沙星中间体3-甲氨基哌啶的合成工艺。6) 3-Aminomethyl piperidine 3-氨甲基哌啶补充资料:(R)-3-氨基哌...