(5aR,10bS)-(+)-5a,10b-Dihydro-2-(pentafluorophenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium tetrafluoroborate, min. 98%,(5aR,10bS)-(+)-5a,10b-二氢-2-(五氟苯基)-4H,6H-茚并[2,1-b][1,2,4]三唑并[4,3-d][1,4]恶唑嗡 四氟硼酸 , min. 98%
(5aR,10bS)-(+)-5a,10b-二氢-2-(五氟苯基)-4H,6H-茚并[2,1-b][1,2,4]三唑并[4,3-d][1,4]恶唑嗡 四氟硼酸 , min. 98%
(5aR,10bS)-(+)-5a,10b-Dihydro-2-(pentafluorophenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium tetrafluoroborate, min. 98%
品牌: Strem
产品编号: 07-0415
分子式: [C??H??F?N?O]?BF
分子量: 467.10
纯度: min. 98%
包装库存价格
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基本信息

安全信息

化学和物理性质

产品描述

Technical Notes:

1.Scope of the asymmetric intramolecular Stetter recation catalyzed by chiral nucleophilic triazolinylideneCarbens

2.Catalytic asymmetric Stetter reaction onto vinyl phosphine oxide and vinyl phosphonates .

3.N-Heterocyclic carbene catalyzed asymmetric hydration: Direct synthesis of a-protio and a-deuterio, a chloro and a-fluoro carboxylic acids

4.Chemoselective conversion of a-unbranched aldehydes to amides, esters and carboxylic acids by NHC-catalysis.

5.Extending the Stetter reaction with 1-6 acceptors .

6.N-Heterocyclic carbene-catalyzed/L ewis acid strategy for the stereoselective synthesis of spirocyclic

oxindole -dihydropyranones.

7.Access to P-stereogenic phosphinatesviaN-heterocycle

carbene- catalyzed desymmetrization of bisphenols.

8.N-Heterocyclic carbene catalyzed intramolecular nucleophilic substitution: Enantioselective construction of all carbon quaternary stereocenters.

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