![(11bR)-8,9,10,11,12,13,14,15-Octahydro-4-hydroxy-2,6-di-1-naphthalenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 95%, (98.5% ee),(11bR)-8,9,10,11,12,13,14,15-八氢-4-羟基-2,6-二-1-萘基-4-氧化物二萘并[2,1-d:1',2'-f][1,3,2]二噁磷杂庚英 , 95%](https://static.jkchemical.com/Structure/246/2463943.png)
(11bR)-8,9,10,11,12,13,14,15-八氢-4-羟基-2,6-二-1-萘基-4-氧化物二萘并[2,1-d:1',2'-f][1,3,2]二噁磷杂庚英 , 95%
(11bR)-8,9,10,11,12,13,14,15-Octahydro-4-hydroxy-2,6-di-1-naphthalenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 95%, (98.5% ee)
分子式: C40H33O4P
分子量: 608.7
纯度: 95%
| 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.Friedel-Crafts Alkylation: Chiral phosphoric acid catalyzed F riedel-Crafts alkylation of indoles with 3,3,3- trifluoropyruvate gave the corresponding adducts in excellent yields with high enantioselectivities.
2.Pinacol Rearrangement: It has been found that indolyl diols can be treated with chiral phosphoric acids to effect a regio- and enantiose lective pinacol rearrangement with high efficiency.
References:
1.Asian J. Chem.. 2010, 5, 470-472.
2. Angew. Chem. Int. Ed., 2010, 49, 9734-9736.
