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(R,R)-3,5-Bistrifluoromethylphenyl-NAS Bromide Maruoka chiral phase-transfer catalyst optically active spiro ammonium salt 100mg Wako
Product code: 029-14921
Pack Size: 100mg
CE Verified: Research Use Only
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Product Information
(R,R)-3,5-Bistrifluoromethylphenyl-NAS Bromide Maruoka chiral phase-transfer catalyst 100mg produced by FUJIFILM Wako Pure Chemical Corporation
Chiral phase-transfer catalysts, which are optically active spiro ammonium salts with 2 binaphthyl rings that allow for easy molecule designing, were invented by Professor Maruoka of the Kyoto University. (R,R)-3,4,5-Trifluorophenyl-NAS Bromide shows high catalytic activity and high enantioselectivity in asymmetric alkylation of alpha-amino acid derivatives 1. By using (R,R)-3,5-Bistrifluoromethylphenyl-NAS Bromide, beta-hydroxy alpha-amino acid derivatives which are important chiral units of biologically active peptides are obtained in good yield by the aldol reaction of glycine derivatives with aldehydes. It was found that erythro isomers, which are major products, were obtained with high enantioselectivity 2.
Features:
1. The rational molecular design of C2-symmetric chiral quaternary ammonium salt
2. Reaction under mild organic / aqueous biphase conditions
3. Catalysing the asymmetric alkylations of alpha-amino acid derivatives and the direct asymmetric aldol reactions of glycine schiff base with aldehydes to the corresponding beta-hydroxy-alpha-amino acid derivatives
References:
1. Ooi T., Takeuchi M., Kameda M. and Maruoka K. : J. Am. Chem. Soc., 122 (21), 5228-5229 (2000).
2. Ooi T., Taniguchi M., Kameda M., Maruoka K. : Angew. Chem. Int.
Molecular Formula=C60H36BrF12N
Molecular Weight=1078.82
Store at room temperature
For organic synthesis
Chiral phase-transfer catalysts, which are optically active spiro ammonium salts with 2 binaphthyl rings that allow for easy molecule designing, were invented by Professor Maruoka of the Kyoto University. (R,R)-3,4,5-Trifluorophenyl-NAS Bromide shows high catalytic activity and high enantioselectivity in asymmetric alkylation of alpha-amino acid derivatives 1. By using (R,R)-3,5-Bistrifluoromethylphenyl-NAS Bromide, beta-hydroxy alpha-amino acid derivatives which are important chiral units of biologically active peptides are obtained in good yield by the aldol reaction of glycine derivatives with aldehydes. It was found that erythro isomers, which are major products, were obtained with high enantioselectivity 2.
Features:
1. The rational molecular design of C2-symmetric chiral quaternary ammonium salt
2. Reaction under mild organic / aqueous biphase conditions
3. Catalysing the asymmetric alkylations of alpha-amino acid derivatives and the direct asymmetric aldol reactions of glycine schiff base with aldehydes to the corresponding beta-hydroxy-alpha-amino acid derivatives
References:
1. Ooi T., Takeuchi M., Kameda M. and Maruoka K. : J. Am. Chem. Soc., 122 (21), 5228-5229 (2000).
2. Ooi T., Taniguchi M., Kameda M., Maruoka K. : Angew. Chem. Int.
Molecular Formula=C60H36BrF12N
Molecular Weight=1078.82
Store at room temperature
For organic synthesis
Specification
- Brand FUJIFILM Wako Chemicals Europe GmbH – Lab Chem
- Sterile N
- CE Certified Research Use Only
- Warranty Period Standard Terms Apply
- Is product classified as dangerous goods? No
- Does the product contain latex? Unspecified
- Source Species NULL
- CAS Number NULL
- Application Organic Synthesis
- Molecular Formula C60H36BrF12N
- Form 100mg
- Concentration NULL
- Purity Min 96% by HPLC
- Marketed Grade NULL
- Molecular Weight 1078.82
- Shelf Life NULL
- Species Reactivity NULL
- Preparation Form White-brown crystalline powder
Storage Details
- Pack Description 100mg
- Shipping Condition Ambient
- Storage Condition Ambient
- Pack Length (m) 0.06
- Pack Width (m) 0.06
- Pack Height (m) 0.06
- Pack Weight (kg) 0.00
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