(S)-Ru(OAc)2(BINAP)

• Catalog No.: 693189
• CAS Number: 261948-85-0
• M. F.: C48H38O4P2Ru
• M. W.: 841.830442

SYNONYMS

• IUPAC name: {1-[2-(diphenylphosphanyl)naphthalen-1-yl]naphthalen-2-yl}diphenylphosphane (acetyloxy)ruthenio acetate
• IUPAC Traditional name: binap (acetyloxy)ruthenio acetate
• Synonyms: 二乙酸根[(S)-(+)-2,2′-二(二苯基膦基)-1,1′-联萘基]钌(II); Diacetato[(S)-(-)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl]ruthenium(II)

DATABASE IDS

• MDL Number: MFCD09753020
• CAS Number: 261948-85-0

PROPERTIES

• Empirical Formula (Hill Notation): C48H38O4P2Ru
• Storage Temperature: 2-8°C

DETAILS

Description (English)

Packaging
100, 500 mg in glass bottle
Legal Information
Sold in collaboration with Takasago for research purposes only.
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Catalyst for:
• Synthesis of zaragozic acid D and formal syntheses of zaragozic acids A and C
• Enantioselective synthesis of the spirocyclic C-arylglycopyranoside (+)-papulacandin D via palladium-catalyzed, organosilanolate-based cross-coupling reaction and a Lewis-base catalyzed, enantioselective allylation reaction
• Asymmetric hydrogenation of 2-formyl-1-methylene-1,2,3,4-tetrahydroisoquinoline
• Asymmetric reduction of (nitro)(phenyl)propene
• Asymmetric synthesis of chiral d-lactones via hydrogenation
• Asymmetric hydrogenation of bis(diphenylphosphinoyl)butadiene

Description (简体中文)

包装
100, 500 mg in glass bottle
Legal Information
与 Takasago 合作销售，仅用于研究目的。日本注册号 1800526
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Catalyst for:
• Synthesis of zaragozic acid D and formal syntheses of zaragozic acids A and C
• Enantioselective synthesis of the spirocyclic C-arylglycopyranoside (+)-papulacandin D via palladium-catalyzed, organosilanolate-based cross-coupling reaction and a Lewis-base catalyzed, enantioselective allylation reaction
• Asymmetric hydrogenation of 2-formyl-1-methylene-1,2,3,4-tetrahydroisoquinoline
• Asymmetric reduction of (nitro)(phenyl)propene
• Asymmetric synthesis of chiral d-lactones via hydrogenation
• Asymmetric hydrogenation of bis(diphenylphosphinoyl)butadiene