跳转至内容
Merck

763039

XantPhos Pd G3

95%, solid

别名:

[(4,5-双(二苯基膦)-9,9-二甲基呫吨)-2-(2 & # 8242;-氨基-1,1 & # 8242;-联苯)]甲磺酸钯(ⅱ)

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式(希尔记法):
C52H45NO4P2PdS
化学文摘社编号:
分子量:
948.35
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


产品名称

XantPhos Pd G3, 95%

Quality Segment

product line

Buchwald precatalyst Generation 3

assay

95%

form

solid

feature

generation 3

reaction suitability

core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst
reaction type: Cross Couplings

mp

164-167 °C (decomposition)

functional group

phosphine

SMILES string

CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.CC3(C)c4cccc(P(c5ccccc5)c6ccccc6)c4Oc7c(cccc37)P(c8ccccc8)c9ccccc9

InChI

1S/C39H32OP2.C12H10N.CH4O3S.Pd/c1-39(2)33-25-15-27-35(41(29-17-7-3-8-18-29)30-19-9-4-10-20-30)37(33)40-38-34(39)26-16-28-36(38)42(31-21-11-5-12-22-31)32-23-13-6-14-24-32;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h3-28H,1-2H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1

InChI key

AJVXPGQYAKUTGX-UHFFFAOYSA-M

General description

XantPhos Pd G3是第三代(G3) Buchwald预催化剂。它具有空气、水分和热稳定特性,高度可溶于各种常见的有机溶剂。它在溶液中有很长的寿命。XantPhos Pd G3是钯催化交叉偶联反应的优良试剂。它的一些独特特征包括催化剂负载量更低、反应时间更短、可有效形成活性催化物质和精确控制配体与钯的比例。

Application

XantPhos Pd G3 可用于以下过程:
  • 帕默内酯(palmerolide)合成过程中的Negishi交叉偶联反应
  • 三乙胺存在的情况下下杂芳基溴化物与一氧化碳(CO)的氨基羰基化反应。
  • 聚糖基硫醇和糖苷配基卤化物之间通过形成C-S键进行偶联。
对于小规模和高通量用途,产品为ChemBeads ((932213


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库


商品

All contents in the foil bag are weighed, plated, packed, and sealed in a glove box under nitrogen.

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。

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 of standard Schlenk technique is recommended.

查看所有文章

A synthetic approach to palmerolides via Negishi cross coupling. The challenge of the C15-C16 bond formation.
Carrillo J, et al.
Tetrahedron Letters, 55(33), 4623-4627 (2014)
Stereoretentive Palladium-Catalyzed Arylation, Alkenylation, and Alkynylation of 1-Thiosugars and Thiols Using Aminobiphenyl Palladacycle Precatalyst at Room Temperature.
Bruneau A, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 21(23), 8375-8379 (2015)
2-Aminobiphenyl Palladacycles: The ?Most Powerful? Precatalysts in C-C and C-Heteroatom Cross-Couplings.
Bruneau A, et al.
ACS Catalysis, 5(2), 1386-1396 (2015)