700762
(S)-SIPHOS-PE
97%
别名:
(11aS)-(-)-10,11,12,13-四氢茚并[7,1-de:1′, 7′-fg][1,3,2]二氧磷-5-双[(R)-1-苯乙基]胺, N-二[(R)-1-苯乙基]-[(S)-1,1′-螺二氢茚-7,7′-二基]亚磷酰胺
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关于此项目
经验公式（希尔记法）:
C33H32NO2P
CAS Number:
分子量:
505.59
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
97%
表单
powder
旋光性
[α]22/D −65.0°, c = 1 in chloroform
mp
120-125 °C
官能团
amine
phenyl
储存温度
−20°C
SMILES字符串
C[C@@H](N([C@H](C)c1ccccc1)P2Oc3cccc4CCC5(CCc6cccc(O2)c56)c34)c7ccccc7
InChI
1S/C33H32NO2P/c1-23(25-11-5-3-6-12-25)34(24(2)26-13-7-4-8-14-26)37-35-29-17-9-15-27-19-21-33(31(27)29)22-20-28-16-10-18-30(36-37)32(28)33/h3-18,23-24H,19-22H2,1-2H3/t23-,24-,33?/m1/s1
InChI key
ZXLQLIDJAURBDD-HRPAVAKOSA-N
应用
(S)-SIPHOS-PE is a chiral spiro phosphoramidate ligand that can be used to synthesize:
- Spiroindolenines by Pd-catalyzed intramolecular dearomative arylation of haloaryl-3-substituted indoles.
- Enantioselective conjugate addition compound by Cu-catalyzed 1,4-addition of diethylzinc (Et2Zn) to cyclic enones.
- Octaketide natural products via rhodium-phosphoramidite catalyzed alkene hydroacylation.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Highly enantioselective copper-catalyzed conjugate addition of diethylzinc to enones using chiral spiro phosphoramidites as ligands
Zhou H, et al.
The Journal of Organic Chemistry, 68(4), 1582-1584 (2003)
Rhodium-phosphoramidite catalyzed alkene hydroacylation: Mechanism and octaketide natural product synthesis
von Delius M, et al.
Journal of the American Chemical Society, 134(36), 15022-15032 (2012)
Palladium (0)-catalyzed dearomative arylation of indoles: convenient access to spiroindolenine derivatives
Wu K-J, et al.
Organic Letters, 14(14), 3772-3775 (2012)
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