所有图片(1)
About This Item
经验公式（希尔记法）:
C48H40P2
CAS号:
分子量:
678.78
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
形式
solid
质量水平
旋光性
[α]20/D -156°, c = 0.5 in benzene
mp
250-255 °C
InChI
1S/C48H40P2/c1-33-13-23-39(24-14-33)49(40-25-15-34(2)16-26-40)45-31-21-37-9-5-7-11-43(37)47(45)48-44-12-8-6-10-38(44)22-32-46(48)50(41-27-17-35(3)18-28-41)42-29-19-36(4)20-30-42/h5-32H,1-4H3
InChI key
IOPQYDKQISFMJI-UHFFFAOYSA-N
应用
( S )-T-BINAP 与硝酸银反应生成 ( S )-Tol-BINAP·AgNO 3 ，可催化醛的对映选择性烯丙基化反应生成对映体纯的仲醇。可作为钯催化的碘芳烃不对称双碳氢化反应中的手性配体，形成 α-氨基酰胺类。它还能催化 邻 - 叔 -丁基苯胺衍生物与碳酸二烯丙酯的不对称 N -烯丙基化反应，生成手性 N -烯丙基 邻 - 叔 -丁基苯胺。
法律信息
与 Takasago 联合销售，仅供研究使用。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Catalytic enantioselective hydroboration of cyclopropenes
Rubina, Marina, Michael Rubin, and Vladimir Gevorgyan
Journal of the American Chemical Society, 125.24, 7198-7199 (2003)
Asymmetric synthesis of a-aminoamides by Pd-catalyzed double carbohydroamination.
Nanayakkara P and Alper H.
Chemical Communications (Cambridge, England), 18, 2384-2385 (2003)
A novel direct catalytic asymmetric synthesis of cyclic indole derivatives by intramolecular carbopalladation of allenes and subsequent intramolecular amination
Hiroi, Kunio, et al.
Tetrahedron Asymmetry, 13.13, 1351-1353 (2002)
New palladium (II)-catalyzed asymmetric 1, 2-dibromo synthesis
El-Qisairi, Arab K., et al.
Organic Letters, 5.4, 439-441 (2003)
An enantioselective Baylis?Hillman reaction catalyzed by chiral phosphines under atmospheric pressure
Hayase, Tadakatsu, et al.
Chemical Communications (Cambridge, England), 12, 1271-1272 (1998)
商品
We present an article concerning BINAP/SEGPHOS® Ligands and Complexes.
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