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4-溴-2,6-二叔丁基苯甲醚 4-Bromo-2,6-Di-Tert-Butylanisole 1516-96-7合成工艺路线路线简述
- 合成目标产物 (Dtbm)2Ph 主要起始原料 (Dtbm)2P(O)H
- (文献来源)合成步骤主要原料 (Dtbm)2P(O)H
📜Bis(3,5-Ditert-Butyl-4-Methoxyphenyl)-Oxophosphanium置于lithium Aluminium Tetrahydride体系中,用 乙醚 用作溶剂,以60%的收率获得二(3,5-二叔丁基-4-甲氧基苯基)膦
参考文献:对映选择性铑催化的原子经济宏观内酯化
标题:对映选择性铑催化的原子经济宏观内酯化
摘要:描述了形成大内酯的高度吸引人的途径,大内酯形成多种多样的天然化合物的环状支架.尽管已经探索了许多针对该结构基序的化学方法,但是环化的不对称变体是前所未有的.在这里,我们通过ω-烯基取代的羧酸的分子内原子-经济铑催化的偶合来呈现对映选择性大内酯化作用.使用改良的二重配体,手性dtbm二联体,可实现高对映选择性(高达93% Ee).该反应可耐受多种功能,包括α,β-不饱和羧酸和二肽,并提供所需的具有高对映体和非对映体选择性的大环.
Doi:10.1002/anie.201604301
海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2905110000-甲醇
2907121100-间甲酚 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-2025096445-A1
优先权日:2023-10-30
标题:Synthesis of intermediates for the preparation of macrocyclic compounds
发明人:CHOI YOUNGGI; HUYNH HOAN
权利人:ALKERMES INC
摘要:Provided are methods for synthesizing intermediates useful in the preparation of compounds having activity against orexin-2 receptor.
专利号:ES-2404827-T3
优先权日:2008-12-18
标 题:Procedure for the synthesis of aminomethyl-tetralin derivatives
专利号:US-9062085-B2
优先权日:2010-09-10
标 题 :Biaryl diphosphine ligands, intermediates of the same and their use in asymmetric catalysis
发明人:ABDUR-RASHID KAMALUDDIN; JIA WENLI; LU SHUIMING; GUO RONGWEI; CHEN XUANHUA; AMOROSO DINO
权利人:ABDUR-RASHID KAMALUDDIN; JIA WENLI; LU SHUIMING; GUO RONGWEI; CHEN XUANHUA; AMOROSO DINO; KANATA CHEMICAL TECHNOLOGIES INC
摘要:The present disclosure relates to biaryl diphosphine ligands of the formula (B), processes for the production of the ligands and the use of the ligands in metal catalysts for asymmetric synthesis. The disclosure also relates to intermediates used for the production of the biaryl diphosphine ligand. (Formula (B))
专利号:MX-2011005793-A
优先权日:2008-12-18
标题:PROCEDURE FOR SYNTHESIS OF AMINO-METHYL TETRALINE DERIVATIVES.
专利号:US-7642357-B2
优先权日:2004-08-27
标 题 :Iridium complexes
发明人:MASHIMA KAZUSHI; YAMAGATA TSUNEAKI
权利人:TAKASAGO PERFUMERY CO LTD
摘要:The present invention has as its object to provide an iridium complex represented by the general formula:n n[(I r H L 1 L 2 ) 2 (μ−X 1 )(μ−X 2 )(μ−X 3 )]X 4   (1)n n(wherein L 1 and L 2 may be the same or different and each represent a monodendate neutral ligand, or each cooperate with the other to form a bidendate neutral ligand; X 1 , X 2 and X 3 may be the same or different, and each represent a halogen atom; and X 4 is a counter-anion). Also, the present invention provides a novel catalyst which can achieve excellent performance as a catalyst for asymmetric synthesis, especially asymmetric hydrogenation, in terms of chemical selectivity, enantioselectivity and catalytic activity, and the like.