![(11bR)-4-Hydroxy-2,6-diphenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee),（11bR）-4-羟基-2,6-二苯基-4-氧化物 - 萘并[2,1-d：1'，2'-f] [1,3,2]二氧磷杂环庚烯，98％，（99％ee）） , 98%](https://static.jkchemical.com/Structure/246/2463945.png)
（11bR）-4-羟基-2,6-二苯基-4-氧化物 - 萘并[2,1-d：1'，2'-f] [1,3,2]二氧磷杂环庚烯，98％，（99％ee）） , 98%
(11bR)-4-Hydroxy-2,6-diphenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee)
分子式: C₃₂H₂₁O₄P
分子量: 500.5
纯度: 98%
| 包装 | 库存 | 价格 | |
|---|---|---|---|
暂无数据 | |||
推荐产品
基本信息
安全信息
化学和物理性质
产品描述
Technical Notes:
1.Diels-Alder Reaction: A highly enantioselective anti. diastereoselective hetero Diels -Alder reaction between a glyoxylate and siloxy- or methoxydienes using a chiral phosphoric acid catalyst that possesses less bulky phenyl groups at the 3 and 3' positions of binaphthyl has been developed.
2.Kinetic Resolution: In the presence of 10 mol% of a chiral phosphoric acid, a variety of racemic N-benzylic sulfonamides having N-(3-indolyI)methyl groups smoothly undergo kinetic resolution with benzyl thiol at 0 'C or at room temperature and the remaining sulfonamides are recovered in moderate to excellent yields and with excellent ee.
References:
1. J. Am. Chem. Soc.. 2009, 131, 12882-12883.
2. Chem. Commun.. 2012, 48, 898 900.
