CAS: 34306-42-8; Boc-Abu-Oh

相似化合物

45121-22-0 77284-64-1 135112-27-5

上下游产品

CAS号1492-24-6 L-2-氨基丁酸 | CAS号24424-99-5 二碳酸二叔丁酯 | CAS号91028-39-6 (S)-2-((叔丁氧羰基)氨... | CAS号58561-08-3 Butanoic acid, ... | CAS号1070-19-5 Carbonazidic ac... | CAS号4530-20-5 B°C-甘氨酸 | CAS号185508-77-4 tert-butyl (2-(... | CAS号150736-72-4 N-B°C-(S)-(-)-2... | CAS号288-32-4 咪唑 | CAS号7682-18-0 DL-2-氨基丁酸甲酯盐酸盐 | CAS号1492-24-6 L-2-氨基丁酸

Boc-L-蛋氨酸置于4-二甲氨基吡啶,Lithium Hydroxide,镍,N,N'-二环己基碳二亚胺体系中,用 四氢呋喃,甲醇,乙醇,二氯甲烷,水 作为反应溶剂,化学反应生成 Boc-L-2-氨基丁酸
参考文献:合成astin,B和c的方法
标题:合成astin,B和c的方法
摘要:合成了两个非必需氨基酸,(+)-(S)-2-氨基丁酸和l-β-苯丙氨酸的甲基酯[(+)-((R)-3-氨基-3-苯基丙酸]提供三肽,可用于合成astin,B和c.
DOI:10.1016/s0040-4039(00)76775-X

专利信息

专利号:US-9242925-B2
优先权日:2011-08-29
标题:Versatile and stereospecific synthesis of γ,δ-unsaturated amino acids by Wittig reaction
发明人：JUGE SYLVAIN; BAYARDON JEROME; REMOND EMMANUELLE; ONDEL-EYMIN MARIE-JOELLE
权利人:JUGE SYLVAIN; BAYARDON JEROME; REMOND EMMANUELLE; ONDEL-EYMIN MARIE-JOELLE; CENTRE NAT RECH SCIENT; UNIV BOURGOGNE
摘要:The γ,δ-unsaturated α-amino acids of general formula (I). Also, a versatile process for the stereospecific synthesis of said compounds of formula (I), involving a Wittig reaction. Further, intermediate products of general formulae (II) and (III), as shown below, which are involved in the synthesis of compounds (I). n n n n n n n n n n n n Compounds of general formula (I) may be useful as therapeutic substances, or as reagents or intermediates for fine chemistry.

专利号:US-2011124867-A1
优先权日:2007-12-18
标题 :Process and intermediates for the Synthesis of heterocyclic Substituted Piperazines with CXCR3 Antagonist Activity
发明人：CHEN FRANK XING; CUTARELLI TIMOTHY D; FU XIAYONG; LIANG XIAN; MCALLISTER TIMOTHY L; ORR ROBERT K; YIN JIANGUO; YONG KELVIN H; ZHU MAN
权利人:SCHERING CORP
摘要:The present invention relates to novel processes for the preparation of the compound of the Formula A45: n n n n n n n n n n or a physiologically acceptable salt, solvate or prodrug thereof, which has utility, for example, as a pharmaceutically active compound with CXCR3 antagonist activity, and to novel intermediates useful in the synthesis thereof.

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-5856107-A
优先权日:1997-02-04
标 题 :Combinatorial libraries of imidazol-pyrido-indole and imidazol-pyrido-benzothiophene derivatives, methods of making the libraries and compounds therein
发明人：OSTRESH JOHN M; HOUGHTEN RICHARD A
权利人:TREGA BIOSCIENCES INC
摘要:The invention provides a rapid approach for combinatorial synthesis and screening of libraries of imidazol-pyrido-indole and imidazol-pyrido-benzothiophene compounds. The present invention further provides methods of preparing the libraries and the individual compounds made by the combinatorial synthesis.

专利号:US-2014364339-A1
优先权日:2011-08-29
标 题 :Versatile and stereospecific synthesis of gamma,delta -unsaturated amino acids by wittig reaction

专利号:US-9567337-B2
优先权日:2013-12-20
标题 :Process methods for phosphatidylinositol 3-kinase inhibitors
发明人：BREMNER STACY; EVARTS JERRY; SUJINO KEIKO; TRAN DUONG; VIZITIU DRAGOS
权利人:GILEAD CALISTOGA LLC
摘要:A process for the synthesis of quinazolinone containing compounds which may be useful for the treatment of cancer, is hereby disclosed. In addition, compound intermediates relating to these processes are also disclosed.