CAS: 104-03-0; 4-Nitrophenylacetic Acid

相似化合物

1197-55-3 100-27-6 5445-26-1

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CAS号555-21-5 4-硝基苯乙腈 | CAS号54075-25-1 BENZENEMETHANOL... | CAS号1197-55-3 对氨基苯乙酸 | CAS号79054-43-6 diethyl (E)-(1-... | CAS号103-82-2 苯乙酸 | CAS号53274-19-4 (p-Nitrophenyl)... | CAS号2945-08-6 对硝基苯乙酸甲酯 | CAS号10565-13-6 2-(4-硝基苯基)丙二酸二乙酯 | CAS号106111-25-5 2-[(4-nitrophen... | CAS号39552-81-3 2-(4-氨基苯基)乙酸甲酯 | CAS号5445-26-1 对硝基苯乙酸乙酯 | CAS号5438-70-0 4-氨基苯乙酸乙酯 | CAS号5339-26-4 4-硝基苯乙基溴 | CAS号15121-86-5 2-(4-nitropheny... | CAS号14064-58-5 1-methoxy-3-[2-... | CAS号20264-90-8 1-(4-NITROPHENY... | CAS号20273-74-9 2-(4-nitropheny...

2,2,2-Trichloro-1-(4-Nitrophenyl)Ethanol置于sodium Tetrahydroborate,二苯基二硒醚,Sodium Hydroxide体系中,用 乙醇 用作溶剂,化学反应 48.0H,以85%的收率获得对硝基苯乙酸
参考文献:醛的一般和实际转化为均聚的羧酸.
标题:醛的一般和实际转化为均聚的羧酸.
摘要:在碱性条件下,醛与三氯甲基甲烷,然后与硼氢化钠或苯基硒基(三乙基)硼酸钠反应,可以高收率得到同系羧酸.该操作简单的过程为其他认证协议提供了一种实用,有效的替代方法.该方法与敏感的醛兼容,包括烯醛和可烯化的醛.它还提供了方便的获取α-单十二烷基羧酸的途径.
Doi:10.1021/ol8016484

专利信息

专利号:US-6133409-A
优先权日:1996-12-19
标 题:Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds
发明人：SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
权利人:AVENTIS PHARM PROD INC
摘要:This invention is directed to a process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and alpha , beta -unsaturated carboxylic acid and aldehyde compounds and to polymeric hydroxylamine resin compounds useful therefor.

专利号:US-7960578-B2
优先权日:2007-03-21
标题:Method for the synthesis of peptides without solvent
发明人：MARTINEZ JEAN; LAMATY FREDERIC; DECLERCK VALERIE
权利人:CENTRE NAT RECH SCIENT; UNIV MONTPELLIER I
摘要:The disclosure relates to a method for the synthesis of a compound of the formula (I) in which: n is an integer higher than or equal to 1; Rb and each Rn are independently a hydrogen atom, a C 1 -C 6 arylalkyl group or a C 1 -C 6 alkyl group substituted or not by an aryl group, —COOH, C 1 -C 6 , —COO-(alkyl), —CONH 2 , —SH, heteroaryl, —NH 2 , —NHC(NH)(NH 2 ), C 1 -C 6 -s-(alkyl), —OH or phenol; Ra is a N-protective group; Rc is a ORd group in which Rd is a C 1 -C 6 alkyl group or a NReRf group in which Re and Rf Re independently an N-protective group.

专利号:EP-0946478-B1
优先权日:1996-12-19
标题 :Process for the solid phase synthesis of aldehydes, ketones and hydroxamic acid compounds
发明人：SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
权利人:AVENTIS PHARMA INC
摘要:This invention is directed to processes for the solid-phase synthesis of aldehydes, ketones, oximes, amines and hydroxamic acid compounds and to polymeric hydroxylamine resin compounds useful therefor.

专利号:US-9206222-B2
优先权日:2009-06-29
标题:Solid phase peptide synthesis of peptide alcohols
发明人：CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN
权利人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN; CENTRE NAT RECH SCIENT
摘要:The present invention relates to the synthesis of depsipeptides on solid phase support. Said depsipeptides are then implicated in a solution phase O—N acyl shift enabling to obtain the corresponding peptide alcohols.

专利号:US-6710208-B2
优先权日:1996-12-19
标题 :Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and α,β-unsaturated carboxylic acid and aldehyde compounds
发明人：SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
权利人:AVENTIS PHARMA INC
摘要:This invention is directed to a process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and α,β-unsaturated carboxylic acid and aldehyde compounds and to polymeric hydroxylamine resin compounds useful therefor.

专利号:US-7109377-B2
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
发明人：SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
权利人:HARVARD COLLEGE
摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.