(S)-SEGPHOS®

• 产品号: 693006
• CAS号: 210169-54-3
• 分子式: C38H28O4P2
• 分子量: 610.574042
• 纯 度: ≥94%

产品别名

• 标题: (S)-SEGPHOS®
• IUPAC标准名: {4-[5-(diphenylphosphanyl)-2H-1,3-benzodioxol-4-yl]-2H-1,3-benzodioxol-5-yl}diphenylphosphane
• IUPAC传统名: {4-[5-(diphenylphosphanyl)-2H-1,3-benzodioxol-4-yl]-2H-1,3-benzodioxol-5-yl}diphenylphosphane
• 别名: (S)-(-)-5,5′-双(二苯基膦)-4,4′-二-1,3-苯并二噁茂; (S)-(-)-5,5′-Bis(diphenylphosphino)-4,4′-bi-1,3-benzodioxole

产品登记号

• CAS号: 210169-54-3
• MDL号: MFCD09753005

产品性质

• Empirical Formula (Hill Notation): C38H28O4P2
• 纯度: ≥94%
• 熔点: 231-235 °C
• 比旋光度: [α]20/D -11°, c = 0.5 in chloroform
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Packaging
50, 100 mg in glass bottle
Legal Information
Sold in collaboration with Takasago for research purposes only. JP Registration No. 3148136
SEGPHOS is a registered trademark of Takasago Intl. Corp.
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Chiral biaryl bisphosphine catalytic ligand used for:
• Rhodium-catalyzed asymmetric formal olefination or cycloaddition of 1,3-dicarbonyl compounds with 1,6-diynes or 1,6-enynes
• Stereoselective preparation of homoallylic alcohols via Ir-catalyzed stereoselective transfer hydrogenative crotylation of an allylic acetate with alcohols or aldehydes
• Regio- and stereoselective preparation of axially chiral arylnaphthalene derivatives via rhodium-catalyzed [2+2+2] cycloaddition of diynes with naphthalenepropynoic acid derivatives
• Diastereo- and enantioselective hydrogenation of α-amino-β-keto ester hydrochlorides catalyzed by an iridium complex
• Preparation of dihydroisoquinolinones via nickel-catalyzed denitrogenative annulation of benzotriazinones with 1,3-dienes and alkenes
• Stereoselective preparation of indanol derivatives via Rh-catalyzed enantioselective alkynylative cyclization of allenyl aldehydes with terminal alkynes

详细说明 (简体中文)

包装
50, 100 mg in glass bottle
Legal Information
与 Takasago 合作销售，仅用于研究目的。日本注册号 3148136
法律信息
SEGPHOS 注册商标 Takasago Intl. Corp.
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Chiral biaryl bisphosphine catalytic ligand used for:
• Rhodium-catalyzed asymmetric formal olefination or cycloaddition of 1,3-dicarbonyl compounds with 1,6-diynes or 1,6-enynes
• Stereoselective preparation of homoallylic alcohols via Ir-catalyzed stereoselective transfer hydrogenative crotylation of an allylic acetate with alcohols or aldehydes
• Regio- and stereoselective preparation of axially chiral arylnaphthalene derivatives via rhodium-catalyzed [2+2+2] cycloaddition of diynes with naphthalenepropynoic acid derivatives
• Diastereo- and enantioselective hydrogenation of α-amino-β-keto ester hydrochlorides catalyzed by an iridium complex
• Preparation of dihydroisoquinolinones via nickel-catalyzed denitrogenative annulation of benzotriazinones with 1,3-dienes and alkenes
• Stereoselective preparation of indanol derivatives via Rh-catalyzed enantioselective alkynylative cyclization of allenyl aldehydes with terminal alkynes