best service, quality anAppearance:yellow Powder Storage:Store in dry, dark and ventilated place. Package:according to the clients requirement Application:It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals,
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inquiryProduct Description CAS 941-69-5 N-Phenylmaleimide Product Description Product Name N-Phenylmaleimide CAS No.
Cas:941-69-5
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inquiry1.1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; ...... Guaranteed purity; 2. Large quantity in stock; 3. Largest manufact
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inquiryISO Appearance: Yellow or light yellow crystal Assay(GC): ≥99.0% Melting point: 86°C~90°C Use: N-Phenylmaleimide (N-PM1) can be used as cross linking agent of natural and synthetic rubbers, as heat-resistant modifier of ABS,PVC,
N-Phenylmaleimide Product Name: N-Phenylmaleimide Molecular Weight: 173.17 CAS NO: 941-69-5 EC NO: 213-382-0 Molecular Formula: C10H7NO2
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
N-Phenylmaleimide Manufacturer Factory CAS 941-69-5 N-Phenylmaleimide Manufacturer High quality Best price In stock factory CAS 941-69-5 N-Phenylmaleimide COA TDS price MSDS Name N-Phenylmaleimide Synonyms 1-Phenyl-1H-pyrrole-2,5-
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inquiryAbout Product Technical Details Mol File: 941
Cas:941-69-5
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inquiryN-Phenylmaleimide Basic information Product Name: N-Phenylmaleimide Synonyms: 1H-Pyrrole-2,5-dione, 1-phenyl-;1H-Pyrrole-2,5-dione,1-phenyl-;1-phenyl-1h-pyrrole-5-dione;5-dione,1-phenyl-
Cas:941-69-5
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
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inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
Cas:941-69-5
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inquiryMolecular Formula:C10H7NO3 Molecular Weight:173.17 CAS No.:941-69-5 ECNO.:213-382-0 Appearance: Yellow or light yellow crystal Assay(GC): ≥99.0% Melting point: 86°C~90°C Use: N-Phenylmaleimide (N-PM1) can be used as cro
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:white powder Storage:Store in sealed containers at cool & dr
Specializing in Intermeidates’ development and production, with fixed assets of RMB 2 million and the land of 10000㎡, and including 20 reactors and testing equipments. Currently our main products: Phenyl salicylate Appearance:Yellow crystal
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inquiry1.In No Less 8 years exporting experience. for clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service"
Cas:941-69-5
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inquiryProduct Name: N-Phenylmaleimide CAS: 941-69-5 MF: C10H7NO2 MW: 173.17 EINECS: 213-382-0 Mol File: 941-69-5.mol N-Phenylmaleimide Structure N-Phenylmaleimide Chemical Properties Melting point 85-87 °C (lit.) Boiling point
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
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inquiryN-Phenylmaleimide CAS: 941-69-5 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermed
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Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Product Detail Minimum Order Qty. 10 Gram
Cas:941-69-5
Min.Order:10 Gram
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Type:Trading Company
inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
Appearance:yellow crystalline powder or needles Storage:Room temperature Package:25kg/drum Application:Chemicals Transportation:Express/Sea/Air Port:Any port in china
Cas:941-69-5
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inquiryOur Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
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inquiryN-phenylmaleamic acid
N-phenyl-maleimide
Conditions | Yield |
---|---|
With sulfuric acid In dimethyl sulfoxide; toluene Cyclization; Heating; | 100% |
With sodium acetate at 80 - 85℃; for 4h; | 85% |
With 1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate In 1-Propyl acetate for 3h; Reflux; | 83% |
Conditions | Yield |
---|---|
Stage #1: aniline With 2,4-dimethyl-6-tert-butylphenol; triethylamine; phosphoric acid; zinc diacetate In xylene for 0.0833333h; Stage #2: maleic anhydride In xylene at 140℃; for 6h; Product distribution / selectivity; | 98% |
With phosphoric acid; 2,4-dimethyl-6-tert-butylphenol; zinc diacetate; silica gel; triethylamine In xylene at 140℃; for 6h; Product distribution / selectivity; Industry scale; | 98% |
Stage #1: maleic anhydride With 2,5-dimethylbenzenesulfonic acid; toluene-4-sulfonic acid In tetrahydrofuran; benzene at 85℃; Stage #2: aniline In tetrahydrofuran; benzene at 85℃; for 1h; Temperature; Reagent/catalyst; Solvent; | 98.75% |
7-phenyl-1,7-diaza-bicyclo<2.2.1>heptane-exo-2,3-exo-5,6-tetracarboxylic acid bisphenylimide
A
N-phenyl-maleimide
B
2,5-diphenyl pyrrolo<3,4-c>pyrazole-(2H,5H)-4,6-dione
Conditions | Yield |
---|---|
at 310℃; under 0.1 Torr; | A 95% B 70% |
7-phenyl-1,7-diaza-bicyclo<2.2.1>heptane-endo-2,3-exo-5,6-tetracarboxylic acid bisphenylimide
A
N-phenyl-maleimide
B
2,5-diphenyl pyrrolo<3,4-c>pyrazole-(2H,5H)-4,6-dione
Conditions | Yield |
---|---|
at 310℃; under 0.1 Torr; | A 95% B 70% |
3-chloro-1-phenylpyrrolidine-2,5-dione
N-phenyl-maleimide
Conditions | Yield |
---|---|
With triethylamine In diethyl ether for 2h; | 85% |
3-phenylcarbamoylacrylic acid
N-phenyl-maleimide
Conditions | Yield |
---|---|
With ammonium peroxodisulfate In 1,4-dioxane; dimethyl sulfoxide at 100℃; for 7h; | 84% |
With sodium acetate; acetic anhydride at 70℃; for 1h; | 72% |
With sodium acetate; acetic anhydride at 100℃; for 0.5h; | 43% |
Conditions | Yield |
---|---|
In toluene at 110℃; under 760.051 Torr; for 8h; | A 83% B 55 mg C 6 mg |
Conditions | Yield |
---|---|
With acetic acid at 100℃; for 1.16667h; | 78% |
Conditions | Yield |
---|---|
With acetic acid at 100℃; for 1.33333h; | 75% |
Conditions | Yield |
---|---|
With oxygen; Rose Bengal lactone In water; N,N-dimethyl-formamide for 18h; Inert atmosphere; Irradiation; | 74% |
N-phenylmaleisoimidium perchlorate
N-phenyl-maleimide
Conditions | Yield |
---|---|
With piperidine; triethylamine In diethyl ether for 10h; | 65% |
With morpholine; triethylamine In diethyl ether for 10h; | 65% |
malic acid
aniline
A
D,L-2-Hydroxy-N-phenylsuccinimide
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
for 0.25h; Condensation; Heating; microwave irradiation; | A 62% B 19% |
Conditions | Yield |
---|---|
Stage #1: 3-phenylcarbamoylacrylic acid; acetic anhydride With sodium acetate at 50℃; for 2h; Inert atmosphere; Stage #2: With water at 70℃; for 2h; Inert atmosphere; | 44% |
Conditions | Yield |
---|---|
With copper diacetate; oxygen; triethylamine; 4 A molecular sieve In dichloromethane at 45℃; for 20h; | 43% |
Conditions | Yield |
---|---|
With triethylamine; 1,2-bis-(diphenylphosphino)ethane; zinc; dibromo[1,2-bis(diphenylphosphino)ethane]nickel(II) In acetonitrile at 80℃; for 36h; | 37% |
C21H19NO3
A
N-phenyl-maleimide
B
1-methoxy-1-methyl-1H-indene
(5aS,5bR,8aR,8bS,8cR)-8b-Methoxy-8c-methyl-7-phenyl-5b,8a,8b,8c-tetrahydro-5aH-7-aza-dicyclopenta[a,cd]indene-6,8-dione
(5aS,5bS,8aS,8bS,8cR)-8b-Methoxy-8c-methyl-7-phenyl-5b,8a,8b,8c-tetrahydro-5aH-7-aza-dicyclopenta[a,cd]indene-6,8-dione
Conditions | Yield |
---|---|
at 80 - 100℃; under 0.08 Torr; | A 31% B 3% C 33% D 21% |
N-Phenyl-endo-6-methyl-8-ethyl-8-azabicyclo<2.2.2>oct-4-en-7-one-1,2-dicarboximide
A
1-Ethyl-3-methyl-2-pyridone
B
N-phenyl-maleimide
N-Phenyl-exo-6-methyl-8-ethyl-8-azabicyclo<2.2.2>oct-4-en-7-one-1,2-dicarboximide
Conditions | Yield |
---|---|
In xylene for 42h; Heating; | A n/a B n/a C 25% |
In xylene for 42h; Product distribution; Heating; convertion of endo into exo isomer; | A n/a B n/a C 25% |
Conditions | Yield |
---|---|
In toluene at 110℃; under 760.051 Torr; for 8h; | A 24% B 14 mg |
N-phenyl-maleamic acid methyl ester
N-phenyl-maleimide
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With 1,4-dioxane; phosphorus pentoxide |
endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione
A
furan
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
In chloroform at 43℃; under 750060 Torr; Kinetics; Thermodynamic data; var.temp. and solv: dioxane; Ea and ΔS(excit.); |
exo-10-acetyl-4-phenyl-4,10-diazatricyclo<5.2.1.02,6>dec-8-ene-3,5-dione
A
N-acetylpyrrole
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 55.8℃; under 750060 Torr; Kinetics; Thermodynamic data; var.temp. and solv: dioxane; Ea and ΔS(excit.); |
A
N-phenyl-maleimide
Conditions | Yield |
---|---|
With aluminium trichloride In benzene at 25℃; Equilibrium constant; distribution constant AlCl3 between the imide and its adduct with anthracene was measured; |
endo-10-benzoyl-4-phenyl-4,10-diazatricyclo<5.2.1.02,6>dec-8-ene-3,5-dione
A
N-benzoylpyrrole
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
In chloroform at 30.7℃; under 750060 Torr; Kinetics; Thermodynamic data; var.temp., pressure and solv: CH2Cl2, AcOEt, MeCN, Me2SO, THF, dioxane; Ea and ΔS(excit.); |
exo-10-benzoyl-4-phenyl-4,10-diazatricyclo<5.2.1.02,6>dec-8-ene-3,5-dione
A
N-benzoylpyrrole
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 71.7℃; under 750060 Torr; Kinetics; Thermodynamic data; var.temp. and solv: dioxane; Ea and ΔS(excit.); |
N-phenyl-c-3,c-4-bis(2-hydroxyphenyl)-r-1,c-2-cyclobutanedicarboximide
A
N-phenyl-maleimide
B
dihydroxy-stilbene
Conditions | Yield |
---|---|
In methanol for 0.5h; Product distribution; Ambient temperature; Irradiation; correlation between photochemical fission and chemical structure; |
Conditions | Yield |
---|---|
Kinetics; Thermodynamic data; Ambient temperature; decomposition, also 80 deg C, ΔG(excit.); |
2,3,5-Triphenyl-tetrahydro-pyrrolo[3,4-d]isoxazole-4,6-dione
A
N-phenyl-maleimide
B
C,N-diphenylnitrone
Conditions | Yield |
---|---|
With lithium perchlorate In diethyl ether at 25℃; Equilibrium constant; various concentrations of LiClO4 (also in the absence of LiClO4); |
3,6-epoxy-N-phenyl-1,2,3,6-tetrahydrophthalimide
A
furan
B
N-phenyl-maleimide
Conditions | Yield |
---|---|
With lithium perchlorate In diethyl ether at 25℃; Equilibrium constant; various concentrations of LiClO4 (also in the absence of LiClO4; |
N-phenyl-maleimide
1,3-diphenylisobenzofuran
2,4,9-triphenyl-(3ac,9ac)-3a,4,9,9a-tetrahydro-4r,9c-epioxido-benzo[f]isoindole-1,3-dione
Conditions | Yield |
---|---|
With ethyl acetate for 0.0166667h; Diels-Alder Cycloaddition; | 100% |
In toluene |
diazomethane
N-phenyl-maleimide
7-Phenyl-2,3,7-triazabicyclo<3.3.0>oct-2-ene-6,8-dione
Conditions | Yield |
---|---|
In diethyl ether for 1h; | 100% |
In diethyl ether for 1h; Ambient temperature; | 80% |
N-phenyl-maleimide
N-benzylidenephenylglycine methyl ester
methyl 2,c-4,7-triphenyl-6,8-dioxo-3,7-diazabicyclo-<3.3.O>octane-r-2-carboxylate
Conditions | Yield |
---|---|
With triethylamine Product distribution; Ambient temperature; effect of solvents, metal salts as catalysts, and time; | 100% |
In perdeuteriopyridine at 110℃; for 1.5h; | 100% |
In toluene for 48h; Heating; | 86% |
N-phenyl-maleimide
1,2,3,4,5-Pentamethyl-cyclopenta-2,4-dienylamine
(1S,2R,6S,7R,10S)-10-Amino-1,7,8,9,10-pentamethyl-4-phenyl-4-aza-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione
Conditions | Yield |
---|---|
In dichloromethane at 22℃; for 3.5h; | 100% |
N-phenyl-maleimide
5-(acetylamino)-1,2,3,4,5-pentamethylcyclopentadiene
N-((1S,2R,6S,7R,10S)-1,7,8,9,10-Pentamethyl-3,5-dioxo-4-phenyl-4-aza-tricyclo[5.2.1.02,6]dec-8-en-10-yl)-acetamide
Conditions | Yield |
---|---|
In dichloromethane at 22℃; for 3.5h; | 100% |
N-phenyl-maleimide
N-phenacylpyridinium bromide
(3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione
Conditions | Yield |
---|---|
With triethylamine In chloroform for 0.166667h; Ambient temperature; | 100% |
N-phenyl-maleimide
pyridinium benzoylmethylide
(3aS,4S,9aR,9bR)-4-Benzoyl-2-phenyl-3a,4,9a,9b-tetrahydro-pyrrolo[3,4-a]indolizine-1,3-dione
Conditions | Yield |
---|---|
In chloroform for 0.166667h; Ambient temperature; | 100% |
N-phenyl-maleimide
1-methoxy-1-trimethylsiloxy-1,3,5-hexatriene
(1,3-Dioxo-2-phenyl-2,3,3a,4,7,7a-hexahydro-1H-isoindol-4-yl)-acetic acid methyl ester
Conditions | Yield |
---|---|
In benzene for 1h; Ambient temperature; | 100% |
N-phenyl-maleimide
2,3-bis<(trimethyksilyl)methyl>-1,3-butadiene
2-phenyl-5,6-di(trimethylsilylmethyl)-3a,4,7,7a-tetrahydro-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
With hydroquinone In toluene Heating; | 100% |
N-phenyl-maleimide
cyclopenta-1,3-diene
N-phenylbicyclo[2.2.1]hept-5-ene-2-endo,3-endo-dicarboximide
Conditions | Yield |
---|---|
In neat (no solvent) at 20℃; for 0.0166667h; Diels-Alder Cycloaddition; | 100% |
With 1-hexyl-3-methylimidazolium tetrafluoroborate; K-10 montmorillonite at 20℃; for 0.0833333h; Diels-Alder reaction; | 99% |
With 3-(n-butoxycarbonyl)-1-methylpyridinium bis(trifluoromethanesulfonyl)imide at 20℃; for 0.166667h; Diels-Alder reaction; diastereoselective reaction; | 97% |
Conditions | Yield |
---|---|
In benzene at 80℃; for 30h; | 100% |
N-phenyl-maleimide
Conditions | Yield |
---|---|
In benzene at 75 - 80℃; for 22h; | 100% |
Conditions | Yield |
---|---|
With acetic anhydride; zinc In toluene at 40 - 86℃; for 48h; Inert atmosphere; chemoselective reaction; | 100% |
With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane; water In toluene at 80℃; for 24h; Schlenk technique; Inert atmosphere; | 99% |
With ammonium formate; acetic acid; palladium on activated charcoal at 110℃; for 0.166667h; Hydrogenation; | 96% |
Conditions | Yield |
---|---|
With polymer supported 1-silyloxy-1,3-butadiene In dichloromethane at 25℃; for 14h; | 100% |
N-phenyl-maleimide
ethyl 3-[(dimethylamino)methyl]-1H-indole-2-acetate
Conditions | Yield |
---|---|
In toluene for 2h; Addition; elimination; Heating; | 100% |
N-phenyl-maleimide
(2Z, 4E)-1,3,6-triacetoxyhexa-2,4-diene
Conditions | Yield |
---|---|
hydroquinone In toluene for 7.5h; Cycloaddition; Heating; | 100% |
N-phenyl-maleimide
tert-butyl-dimethyl-[1-methylene-3-(2-nitro-phenyl)-allyloxy]-silane
Conditions | Yield |
---|---|
In benzene at 20℃; for 72h; Cycloaddition; Diels-Alder reaction; | 100% |
N-phenyl-maleimide
Conditions | Yield |
---|---|
In toluene at 80℃; for 20h; Diels-Alder reaction; | 100% |
N-phenyl-maleimide
(R,E)-3-(tert-butyldimethylsiloxy)-1-(4-phenyl-2-oxazolidinon-3-yl)-1,3-butadiene
(3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione
Conditions | Yield |
---|---|
In toluene at -45 - 20℃; for 24h; Diels-Alder reaction; | 100% |
N-phenyl-maleimide
2-(1,2,3,4,5-pentamethyl-cyclopenta-2,4-dienyl)-4,5-dihydro-oxazole
Conditions | Yield |
---|---|
In tetrachloromethane at 25℃; Diels-Alder reaction; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 5h; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 3.5h; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 5h; | 100% |
(-)-(S)-2-(E)-4-(Z)-5-phenyl-4-(p-tolylsulfinyl)penta-2,4-dien-1-ol
N-phenyl-maleimide
(+)-(3aR,4S,7S,7aR,SS)-7-(hydroxymethyl)-2,4-diphenyl-5-(p-tolylsulfinyl)-3a,4,7,7a-tetrahydro-2H-isoindole-1,3-dione
Conditions | Yield |
---|---|
In toluene at 20℃; for 72h; Diels-Alder cycloaddition; | 100% |
Conditions | Yield |
---|---|
In tetrachloromethane at 25℃; Diels-Alder reaction; | 100% |
N-phenyl-maleimide
Conditions | Yield |
---|---|
With H(1+) In perchloric acid aq. HClO4; to the soln. of Co-compd. in aq. HClO4 was added an org. compd.; after 1-2 h the soln. was dild. with H2O; the react. mixt. was absorbed onto an ion-exchange column; washing with aq. HClO4, elution with NaClO4 (pH 2);; Ba(NO3)2 and K2SO4 were added; KClO4 and BaSO4 were removed by fitration; the soln. was condensed by rotoevapn. at 30°C and was filtered; addn. of HClO4, standing overnight at 8°C; recrystn. from HClO4, cooling for 4 h at the same temp.;; | 100% |
N-phenyl-maleimide
3-[1'-(tert-butyldimethylsilyloxy)ethyl]-4-[1-methyleneprop-2-enyl]azetidin-2-one
5-{(2S,3S)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-oxoazetidin-2-yl}-2-phenyl-3a,4,7,7a-tetrahydroisoindole-1,3-dione
Conditions | Yield |
---|---|
With indium(III) chloride In acetonitrile at 20℃; for 48h; Diels-Alder Reaction; | 100% |
N-phenyl-maleimide
cyclopentanealdehyde
(S)-1-(2,5-dioxo-1-phenylpyrrolidin-3-yl)cyclopetanecarboxaldehyde
Conditions | Yield |
---|---|
With (S)-3-amino-3-phenylpropanoic acid; caesium carbonate In dichloromethane at 20℃; for 48h; Michael Addition; enantioselective reaction; | 100% |
With NH2-Phg-(D-Pro)-Gly-Leu-OH In acetonitrile at 20℃; for 72h; Michael Addition; enantioselective reaction; | 95% |
Stage #1: cyclopentanealdehyde With dmap; tert-butyl (2S,3R)-2-amino-3-hydroxybutanoate; SULFAMIDE In dichloromethane at 23℃; for 0.0333333h; Michael addition; Stage #2: N-phenyl-maleimide In dichloromethane at 23℃; for 16h; Michael addition; optical yield given as %ee; enantioselective reaction; | 93% |
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