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Cross coupling

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facet applications:Cross coupling
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Salen配体
Salen配体:Jacobsen和Katsuki在1990年分别发表了第一篇关于salen作为锰的配体用于不对称环氧化反应的报道。
G3和G4 Buchwald预催化剂
G3和G4 Buchwald预催化剂是一类最新的空气、湿度和热稳定型交叉偶联复合物,可用于键形成以实现其多功能性和高反应性。
C2型轴对称手性双噁唑啉(BOX)配体
使用络合Cu(I)OTf的BOX配体进行不对称催化苯乙烯合成氮杂环丙烷的反应,BOX配体带苯基取代基的优于具有位阻需求的叔丁(t-Bu)基团。
用2-甲基吡啶-甲硼烷复合物进行还原胺化反应
2-甲基吡啶-甲硼烷(pic-BH3)是还原胺的一个出色的替代试剂。
TPGS-750-M:用于室温下水中有机金属化学反应的第二代两亲物
Lipshutz及其同事最近开发了第二代技术,用于基于聚氧乙戊基-α-生育酚琥珀酸酯衍生物TPGS-750-M的原始PTS表面活性剂。
金鸡纳生物碱
不对称相转移催化(PTC)已被公认为是许多均相合成有机转化的“绿色”替代方法,并且已被广泛应用。合成修饰的金鸡纳生物碱是用于不对称PTC的典型手性有机催化剂。
N-杂环卡宾-铜络合物
设计全新的金属催化络合物时,N-杂环卡宾配体(NHCs)是绝佳选择。这些催化剂具有空气和水分稳定性,可作为前体用于合成更多空气敏感复合物。
N-杂环卡宾(NHC)配体
随着金属络合物催化的未活化底物的交叉偶联反应领域的快速进展,通过引入大量的非手性和手性膦配体化合物库,已变革了化学市场。
Salen Ligands
Salen Ligands: In 1990, Jacobsen and Katsuki independently published the first reports of salen used as ligands with manganese for asymmetric epoxidation reactions.
N-Heterocyclic Carbene-Copper Complexes
N-Heterocyclic Carbene-Copper Complexes
Chiral Disulfonimides for Asymmetric Counteranion-directed Catalysis (ACDC)
Asymmetric counteranion-directed catalysis (ACDC) has a number of valuable applications in enantioselective synthesis.
Reductive amination with 2-picoline-borane complex
2-picoline-borane (pic-BH3) is an excellent alternative reagent for reductive aminations.
Palladacycle Coupling Catalysts
Palladacyclic catalysts developed by Bedford’s group are examples of a select group of catalysts capable of affecting a variety of coupling reactions using difficult to activate aryl chlorides at very low catalyst loadings.
Aminophosphine Ligands
Aminophosphine Ligands
Scale-Up Guide: Buchwald-Hartwig Amination Reaction
All of the preformed catalysts used in the kit are air and moisture stable complexes in their commercially available form. Once activated by base under the reaction conditions they become sensitive to air. To best enable scale-up success, the use
Diazaphospholane Ligands for Catalytic Asymmetric Transformations
Diazaphospholane Ligands for Catalytic Asymmetric Transformations: Professor Landis and co-workers developed a series of new ligands based on chiral 3,4-diazaphospholane structures.
Umicore Precatalysts
We are happy to offer a series of precatalysts for asymmetric catalysis and Pd based cross coupling catalysis. Our partnership with Umicore allows us to offer a portfolio of metal complexes with batch-to-batch consistency for a plethora of catalytic reactions.
DuPhos and BPE Ligands
Asymmetric hydrogenation reactions represent the ideal process for the commercial manufacture of single-enantiomer compounds, because of the ease by which these robust procedures can be scaled up and because of the low levels of byproducts generated in these asymmetric hydrogenations.
Buchwald Phosphine Ligands
Buchwald Phosphine Ligands
Buchwald GT Capsules for Cross-Coupling
The advent of the Buchwald portfolio of ligands and complexes for cross-coupling reactions in the past decade has greatly advanced the ease of performing this transformation.
Takasago Ligands
Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago
Trialkylphosphine for Morita-Baylis Hillman Reactions
The use of amines and phosphines in nucleophilic catalysis is well precedented; however, arguably one of the severe limitations with respect to exploiting the more nucleophilic, yet less basic, phosphine in this regard is its air sensitivity.
Catalysts for Carbonylation
Professor Geoffrey Coates and co-workers at Cornell University have reported the preparation and use of catalysts composed of an oxophilic Lewis acid and a cobalt tetracarbonyl anion for the ring expansive carbonylation of epoxides to b-lactones and b-lactones to succinic
Cationic Gold(I) Complexes Based on Bulky Phosphine Ligands: New Opportunity for Efficient Gold Catalysis
Cationic Gold(I) Complexes Based on Bulky Phosphine Ligands: New Opportunity for Efficient Gold Catalysis
Hayashi Catalysts
We pleased to offer the latest technology from Hayashi, including both the pre-catalysts.
Nok – Third-Generation Amphiphile for Cross-Coupling Chemistry in Water
Micellular catalysis has provided the ability to carry out several commonly used transformations used in the synthetic community to be carried out in water.
Carreira DOLEFIN Ligands
The selective preparation of diarylmethine stereogenic centers is a challenging endeavor in chemical synthesis, especially when there is little differentiation between the two aryl groups
Gold Catalyst
We are proud to offer a treasure-trove of gold precatalysts and silver salts, as well as an extensive portfolio of unsaturated building blocks to accelerate your research success in this exciting field.
Shvo’s Catalyst
Efficient epimerization catalyst for enzyme mediated dynamic kinetic resolution (DKR).
2nd Generation Buchwald Precatalysts
Buchwald precatalysts and ligands are bulky electron-rich dialkylbiaryl phospine-based catalysts and structurally related ligands that improve reactivity in Pd-catalyzed cross - coupling reactions
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