跳转至内容
Merck
所有图片(1)

主要文件

查看所有文档

693537

Sigma-Aldrich

R-MOP

≥94%

别名:

(R)-(+)-2-(二苯基膦)-2′-甲氧基-1,1′-联萘

登录查看公司和协议定价
所有图片(1)

About This Item

经验公式（希尔记法）:
C33H25OP
CAS号:
145964-33-6
分子量:
468.52
MDL號碼:
MFCD00269686
分類程式碼代碼:
12352005
PubChem物質ID:
329761598

化驗

≥94%

形狀

solid

光學活性

[α]20/D +94°, c = 0.5 in chloroform

SMILES 字串

COc1ccc2ccccc2c1-c3c(ccc4ccccc34)P(c5ccccc5)c6ccccc6

InChI

1S/C33H25OP/c1-34-30-22-20-24-12-8-10-18-28(24)32(30)33-29-19-11-9-13-25(29)21-23-31(33)35(26-14-4-2-5-15-26)27-16-6-3-7-17-27/h2-23H,1H3

InChI 密鑰

KRWTWSSMURUMDE-UHFFFAOYSA-N

一般說明

R-MOP是以双萘为主链的膦配体。

應用

用于不对称反应的Takasago配体和复合物

配体用于钯催化烯烃的不对称硅氢化反应 、钯催化烯丙基酯的还原反应 、铑催化的不对称加成反应 和铜 (Ⅰ) 配合物催化的不对称胺化反应 。

法律資訊

与 Takasago 联合销售，仅供研究之用。US5231202

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKBJ0441V
03502EJ
02704MH

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。

搜索COA

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

Gaku Hattori et al.
Journal of the American Chemical Society, 132(30), 10592-10608 (2010-07-14)
The scope and limitations of the copper-catalyzed propargylic amination of various propargylic esters with amines are presented, where optically active diphosphines such as Cl-MeO-BIPHEP and BINAP work as good chiral ligands. A variety of secondary amines are available as nucleophiles
T Hayashi
Accounts of chemical research, 33(6), 354-362 (2000-07-13)
Chiral monophosphines, whose chirality is due to biaryl axial chirality, have been prepared from enantiomerically pure 2, 2'-dihydroxy-1,1'-binaphthyl and demonstrated to be highly efficient chiral ligands for transition-metal-catalyzed organic transformations, especially for reactions where chelating bisphosphine ligands cannot be used.
Uozomi, Y.
Journal of the American Chemical Society, 9887-9887 (1991)
Rhodium-catalyzed asymmetric addition of aryl- and alkenylboronic acids to isatins.
Ryo Shintani et al.
Angewandte Chemie (International ed. in English), 45(20), 3353-3356 (2006-04-06)
A new optically active monodentate phosphine ligand, (R)-(+)-3-diphenylphosphino-3'-methoxy-4,4'-biphenanthryl (MOP-phen): preparation and use for palladium-catalyzed asymmetric reduction of allylic esters with formic acid
Hayashi, T.
Synthesis, 526-532 (1994)
查看所有相关文献

商品

Chiral Diene Ligands for Asymmetric Transformations

In the last few years, a number of chiral diene ligands have emerged for a variety of asymmetric transformations.1 This powerful new method has proven to be an efficient way for the construction of enantioenriched compounds from achiral substrates.

Chiral Diene Ligands for Asymmetric Transformations

In the last few years, a number of chiral diene ligands have emerged for a variety of asymmetric transformations.1 This powerful new method has proven to be an efficient way for the construction of enantioenriched compounds from achiral substrates.

Takasago Ligands

Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago

Takasago Ligands

Hydrogenation, Asymmetric Catalysis, Binap, SEGPHOS®, Aldol reaction, Alkenylation, Arylation, Mannich reaction, Fluorination, Michael addition, Hydrosilylation, Cycloaddition, Takasago

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门