跳转至内容
Merck

676403

Sigma-Aldrich

(R,R)-(–)-2,3-双(叔丁基甲基膦基)喹喔啉

≥95%

别名:

(R) QuinoxP®

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C18H28N2P2
分子量:
334.38
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥95%

形狀

solid

mp

100-104 °C

官能基

phosphine

SMILES 字串

CP(c1nc2ccccc2nc1P(C)C(C)(C)C)C(C)(C)C

InChI

1S/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/m0/s1

InChI 密鑰

DRZBLHZZDMCPGX-VXKWHMMOSA-N

一般說明

(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline is an air-stable C2-symmetric P-stereogenic phosphine ligand.

應用

在合成转化反应中显示高水平手性控制的高效配体,转化反应范围从金属催化芳基硼酸 1,4-加成到烷基化的开环到不对称氢化。

特點和優勢

Advantages of the QuinoxP* Ligands:
  • It is not oxidized nor epimerized at ambient conditions in air
  • Enantioselectivities are outstanding for various reaction paradigms
  • Hydrogenations proceed under mild reaction conditions
  • Low catalyst loadings yield high TONs

引用

Fang P and Hou XL. "Asymmetric Copper-Catalyzed Propargylic Substitution Reaction of Propargylic Acetates with Enamines." Organic letters 11.20 (2009): 4612-4615.
Imamoto T, et al. "Highly enantioselective hydrosilylation of simple ketones catalyzed by rhodium complexes of P-chiral diphosphine ligands bearing tert-butylmethylphosphino groups." Tetrahedron: Asymmetry 17(4) (2006): 560-565.
Yahav-Levi A, et al. "Aryl-bromide reductive elimination from an isolated Pt (IV) complex." Chemical Communications 46(19) (2010): 3324-3326.

法律資訊

QuinoxP is a registered trademark of Nippon Chemical Industry Co., Ltd.

象形圖

Skull and crossbones

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


从最新的版本中选择一种:

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

A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions.
Ji Y, et al.
Chemical Science (2017)
Optimization of the Preparation of (R)-3, 5-Bis (trifluoromethyl)-?-methyl-N-methylbenzylamine l-(?)-Malic Acid Salt through Classical Resolution.
Brandel CM, et al.
Organic Process Research & Development, 19(12), 1954-1965 (2015)
Rhodium?Catalyzed Dynamic Kinetic Asymmetric Allylation of Phenols and 2?Hydroxypyridines.
Li C and Breit B
European Journal of Chemistry, 22(41), 14655-14663 (2016)
Highly enantioselective hydrosilylation of simple ketones catalyzed by rhodium complexes of P-chiral diphosphine ligands bearing tert-butylmethylphosphino groups.
Imamoto T, et al.
Tetrahedron Asymmetry, 17(4), 560-565 (2006)
Enantioselective Nitroso Aldol Reaction Catalyzed by a Chiral Phosphine?Silver Complex.
Yanagisawa A, et al.
European Journal of Organic Chemistry, 2016(32), 5355-5359 (2016)

商品

QuinoxP*: Air-Stable and Highly Efficient and Productive Chiral Ligands

QuinoxP*: Air-Stable and Highly Efficient and Productive Chiral Ligands

AEM3-944 | UAT | Prefill feature for related product categories not working

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