CAS: 615-58-7; 2,4-Dibromophenol

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CAS号108-95-2 苯酚 | CAS号106-41-2 对溴苯酚 | CAS号1529-17-5 三甲基苯氧基硅 | CAS号4203-50-3 2-苯氧基四氢吡喃 | CAS号95-56-7 2-溴苯酚 | CAS号108-88-3 甲苯 | CAS号2446-83-5 偶氮二甲酸二异丙酯 | CAS号108-94-1 环己酮 | CAS号100-66-3 苯甲醚 | CAS号118-79-6 三溴苯酚 | CAS号55082-33-2 5-溴-2-羟基二苯甲酮 | CAS号89899-44-5 (3-bromo-4-hydr... | CAS号111277-24-8 2-hydroxy-3,5-d... | CAS号26733-16-4 Methanone, (3,5... | CAS号55745-70-5 2,3-二氢苯并呋喃-5-甲醛 | CAS号34133-58-9 2,4-二氰基苯酚 | CAS号4186-54-3 α,3,5-三溴-2-羟基甲苯 | CAS号90-59-5 3,5-二溴水杨醛 | CAS号2183-54-2 2,4-二溴-6-(羟基甲基)苯酚

苯甲酸苯酯置于五溴化磷体系中,化学反应生成 2,4-二溴苯酚
参考文献:Authenrieth; Muehlinghaus,Chemische Berichte,1907,Vol. 40,P. 748
标题:Authenrieth; Muehlinghaus,Chemische Berichte,1907,Vol. 40,P. 748

专利信息

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:WO-2018232298-A1
优先权日:2017-06-16
标题:Anti-fungals compounds targeting the synthesis of fungal sphingolipids

专利号:US-2020207705-A1
优先权日:2017-06-16
标题 :Anti-fungals compounds targeting the synthesis of fungal sphingolipids

专利号:WO-9615111-A1
优先权日:1994-11-15
标 题:Method and intermediates for the synthesis of korupensamines

专利号:US-2024124392-A1
优先权日:2017-06-16
标 题:Anti-fungals compounds targeting the synthesis of fungal sphingolipids

专利号:US-5543523-A
优先权日:1994-11-15
标 题 :Method and intermediates for the synthesis of korupensamines
发明人：HOYE THOMAS R
权利人:UNIV MINNESOTA
摘要:Activated isoquinolines and naphthalenes are disclosed which are useful to prepare korupensamines, michellamines and analogs thereof.