Mango Powder Specification: Name: Mango Powder Identification Standardization Aspect brown fine powder
Hangzhou DaAppearance:yellow powder Storage:Store in dry, dark and ventilated place. Package:according to the clients requirement Application:MAO inhibitor Transportation:by air or by sea Port:Shanghai
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inquiryItems Standard Result Physicochemical Appearance Off-white to yellowish powder Conform
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inquirySuperiority KONO is a leading manufacturer and supplier of chemicals in China. We develop ,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals. We could give you: 1.Best quality
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Name:Mangiferin Alias: Mango glycoside 、 Damuning English Name:Mangiferin CSA:4773-96-0 Molecular formula:C19H18O11 Molecular weight:422.35 Packaging Specification: 25kg/drum high purity 99%min stock Hubei DiBo Chemical Co., Ltd. was foun
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inquiryDensity: 1.843 ± 0.06 g/cm3 (Predicted) Melting point: 269-270 ° C Boiling point: 842.7 ± 65.0 ° C (Predicted) Specific rotation:+43.3 ° (c=0.9, pyridine) Flash point: 303.6 ° C Steam pressure: 3.67E-30mmHg at 25 ° C
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inquiryOur company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryName: Xanthone-c-glucoside Synonyms: mangiferin CAS:4773-96-0 MF: C19H18O11 Appearance: Light yellow power Storage:Store in cool and dry place, away from sun light. Package:25kg/drum Application:Health Food Transportation:By sea or by air
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inquiry1.No Less 8 years exporting experience. 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" Upbio is Specialized
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inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the
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inquirymangiferin CAS:4773-96-0 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 intermediates,
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inquiry1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures
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inquiryPRODUCT DETAILS
Cas:4773-96-0
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inquiryShanghai SOYOUNG onsite assessment conducted by Bureau Veritas commissioned at June 2018. Assessed Supplier of Shanghai SOYOUNG is a faithful and professional supplier of health raw materials in pharmacy, food, cosmetic and other fields for many ye
Cas:4773-96-0
Min.Order:25 Kilogram
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inquiry1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered
Chengdu Biopurify Phytochemicals Ltd. is a leading company in the research, development, manufacture and marketing of High Quality Phytochemicals and Extracts(especially Active Ingredients from Traditional Chinese Medicine,Traditional Chinese Medic
Triumph has the complete production of G- KG - MT service chain,we can make the new technology into productivity quickly in the research and development of new products. Main Business Custom Synthesis: Trading(Raw Mater
Company Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
2-C-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-6-methoxy-1,3,7-trihydroxyxanthone
mangiferin
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane at 0 - 20℃; | 94% |
mangiferin
Conditions | Yield |
---|---|
With 10% palladium hydroxide on charcoal; hydrogen In methanol at 20℃; under 760.051 Torr; for 48h; | 90% |
3-glucosyl-2,3′,4,4′,6-pentahydroxybenzophenone
A
4-β-D-glucopyranosyl-1,3-6,7-tetrahydroxy-9H-xanthen-9-one
B
mangiferin
Conditions | Yield |
---|---|
With sodium carbonate; potassium hexacyanoferrate(III) In water for 1.5h; Ambient temperature; | A 12 mg B 7 mg |
With sodium carbonate; potassium hexacyanoferrate(III) In water for 1.5h; Product distribution; Ambient temperature; | A 12 mg B 7 mg |
Conditions | Yield |
---|---|
In water at 37℃; tannase; |
mangiferin
Conditions | Yield |
---|---|
With hydrogenchloride In water at 100℃; for 1h; Product distribution; other reagent (2N NaOH); other temp.; |
maclurin 3-C-(6''-O-p-hydroxybenzoyl)-β-D-glucoside
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 20 mg / H2O / 35 °C / hesperidinase 2: 7 mg / K3, Na2CO3 / H2O / 1.5 h / Ambient temperature View Scheme |
maclurin 3-C-(2''-O-p-hydroxybenzoyl-6''-O-galloyl)-β-D-glucoside
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 40 mg / H2O / 37 °C / hesperidinase 2: 7 mg / K3, Na2CO3 / H2O / 1.5 h / Ambient temperature View Scheme |
maclurin 3-C-(2''-O-galloyl-6''-O-p-hydroxybenzoyl)-β-D-glucoside
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: H2O / 0.5 h / 37 °C / tannase 2: 20 mg / H2O / 35 °C / hesperidinase 3: 7 mg / K3, Na2CO3 / H2O / 1.5 h / Ambient temperature View Scheme |
Conditions | Yield |
---|---|
In ethanol at 25℃; for 2h; Kinetics; Wavelength; |
3-glucosyl-2,3′,4,4′,6-pentahydroxybenzophenone
mangiferin
Conditions | Yield |
---|---|
With ethylenediaminetetraacetic acid; NADPH at 30℃; for 2h; Enzymatic reaction; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: UDP; Mangifera indica C-glycosyltransferase / 12 h / Enzymatic reaction 2: NADPH; ethylenediaminetetraacetic acid / 2 h / 30 °C / Enzymatic reaction View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Mangifera indica C-glycosyltransferase / 12 h / Enzymatic reaction 2: NADPH; ethylenediaminetetraacetic acid / 2 h / 30 °C / Enzymatic reaction View Scheme |
2,3,4,6-Tetra-O-benzyl-D-glucopyranose
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 10 steps 1.1: pyridine / 12 h / 20 °C 2.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 3.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 4.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 4.2: 1 h / -40 °C / Inert atmosphere 5.1: manganese(IV) oxide / dichloromethane / 36 h 6.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 8.1: caesium carbonate / methanol / 12 h / 80 °C 9.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 10.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 14 steps 1.1: boron trifluoride diethyl etherate / dichloromethane / 12 h / 20 °C / Inert atmosphere 2.1: sodium methylate / methanol / 1 h / 20 °C / pH 11 - 12 3.1: sodium hydride / N,N-dimethyl-formamide / 12 h / 0 - 20 °C 4.1: N-Bromosuccinimide; water / acetone / 3 h / 20 °C / Darkness 5.1: pyridine / 12 h / 20 °C 6.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 7.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 8.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 8.2: 1 h / -40 °C / Inert atmosphere 9.1: manganese(IV) oxide / dichloromethane / 36 h 10.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 11.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 12.1: caesium carbonate / methanol / 12 h / 80 °C 13.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 14.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 2.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 3.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 3.2: 1 h / -40 °C / Inert atmosphere 4.1: manganese(IV) oxide / dichloromethane / 36 h 5.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 7.1: caesium carbonate / methanol / 12 h / 80 °C 8.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 9.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12.5 h / 0 - 20 °C 2.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 12 h / 20 °C 3.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 3.2: 1 h / -40 °C / Inert atmosphere 4.1: manganese(IV) oxide / dichloromethane / 36 h 5.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 7.1: caesium carbonate / methanol / 12 h / 80 °C 8.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 9.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
1,2,4-tris(methoxymethoxy)benzene
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 12 h / 20 °C 2.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 2.2: 1 h / -40 °C / Inert atmosphere 3.1: manganese(IV) oxide / dichloromethane / 36 h 4.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 6.1: caesium carbonate / methanol / 12 h / 80 °C 7.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 8.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 1.2: 1 h / -40 °C / Inert atmosphere 2.1: manganese(IV) oxide / dichloromethane / 36 h 3.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 5.1: caesium carbonate / methanol / 12 h / 80 °C 6.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 7.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
1,3,5-tri-O-benzyl-2-C-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)benzene
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 2.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 2.2: 1 h / -40 °C / Inert atmosphere 3.1: manganese(IV) oxide / dichloromethane / 36 h 4.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 6.1: caesium carbonate / methanol / 12 h / 80 °C 7.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 8.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
p-tolyl-2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 13 steps 1.1: sodium methylate / methanol / 1 h / 20 °C / pH 11 - 12 2.1: sodium hydride / N,N-dimethyl-formamide / 12 h / 0 - 20 °C 3.1: N-Bromosuccinimide; water / acetone / 3 h / 20 °C / Darkness 4.1: pyridine / 12 h / 20 °C 5.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 6.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 7.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 7.2: 1 h / -40 °C / Inert atmosphere 8.1: manganese(IV) oxide / dichloromethane / 36 h 9.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 10.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 11.1: caesium carbonate / methanol / 12 h / 80 °C 12.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 13.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 1.2: 1 h / -40 °C / Inert atmosphere 2.1: manganese(IV) oxide / dichloromethane / 36 h 3.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 5.1: caesium carbonate / methanol / 12 h / 80 °C 6.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 7.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: manganese(IV) oxide / dichloromethane / 36 h 2: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 3: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 4: caesium carbonate / methanol / 12 h / 80 °C 5: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 6: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 3: caesium carbonate / methanol / 12 h / 80 °C 4: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 5: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 2: caesium carbonate / methanol / 12 h / 80 °C 3: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 4: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: caesium carbonate / methanol / 12 h / 80 °C 2: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 3: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 2: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 12 steps 1.1: sodium hydride / N,N-dimethyl-formamide / 12 h / 0 - 20 °C 2.1: N-Bromosuccinimide; water / acetone / 3 h / 20 °C / Darkness 3.1: pyridine / 12 h / 20 °C 4.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 5.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 6.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 6.2: 1 h / -40 °C / Inert atmosphere 7.1: manganese(IV) oxide / dichloromethane / 36 h 8.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 9.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 10.1: caesium carbonate / methanol / 12 h / 80 °C 11.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 12.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
p-methylphenyl 2,3,4,6-tetra-O-benzyl-thio-β-D-glucopyranoside
mangiferin
Conditions | Yield |
---|---|
Multi-step reaction with 11 steps 1.1: N-Bromosuccinimide; water / acetone / 3 h / 20 °C / Darkness 2.1: pyridine / 12 h / 20 °C 3.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane; tetrahydrofuran / 1 h / 0 °C / Inert atmosphere 4.1: trichlorophosphate / 16 h / 20 °C / Inert atmosphere 5.1: n-butyllithium / tetrahydrofuran / 1 h / -40 °C / Inert atmosphere 5.2: 1 h / -40 °C / Inert atmosphere 6.1: manganese(IV) oxide / dichloromethane / 36 h 7.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 8.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C 9.1: caesium carbonate / methanol / 12 h / 80 °C 10.1: toluene-4-sulfonic acid / methanol / 0.5 h / 80 °C 11.1: 10% palladium hydroxide on charcoal; hydrogen / methanol / 48 h / 20 °C / 760.05 Torr View Scheme |
Conditions | Yield |
---|---|
With sodium acetate; acetic acid at 120℃; for 3.5h; | 93.6% |
mangiferin
Conditions | Yield |
---|---|
With calcium hydroxide In dimethyl sulfoxide; glycerol Product distribution / selectivity; | 90.4% |
With potassium hydrogencarbonate In ethanol; water Product distribution / selectivity; | 82.1% |
mangiferin
mangiferin-3-monosodium
Conditions | Yield |
---|---|
With sodium carbonate In ethanol; water Product distribution / selectivity; | 81.7% |
mangiferin
mangiferin-3-monopotassium
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In ethanol; water Product distribution / selectivity; | 78.1% |
acetic anhydride
mangiferin
1,3,6,7-tetra-O-acetyl-2-C-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)xanthone
Conditions | Yield |
---|---|
With iodine at 130℃; for 0.25h; Microwave irradiation; | 78% |
With pyridine at 20℃; for 36h; |
mangiferin
Conditions | Yield |
---|---|
Stage #1: mangiferin With sodium hydrogencarbonate In water; dimethyl sulfoxide at 85℃; Stage #2: With calcium chloride In water; dimethyl sulfoxide at 20℃; Reagent/catalyst; | 74.5% |
mangiferin
Conditions | Yield |
---|---|
With potassium carbonate In water; dimethyl sulfoxide at 60℃; Temperature; | 60.2% |
mangiferin
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; dimethyl sulfoxide at 85℃; Temperature; Reagent/catalyst; | 50.5% |
Conditions | Yield |
---|---|
With triethylamine In ethanol at 65℃; for 5h; pH=7.5; | 46% |
Conditions | Yield |
---|---|
With hydrogen iodide; phenol for 7h; Heating; | 43% |
With hydrogenchloride; recorcinol In water for 6h; Reagent/catalyst; Reflux; | |
With hydrogenchloride; recorcinol In water at 150℃; for 6h; Reagent/catalyst; Green chemistry; |
Conditions | Yield |
---|---|
With triethylamine In methanol; ethanol at 65℃; for 6h; pH=7.5; | 40% |
Conditions | Yield |
---|---|
With pyridine at 20℃; for 20h; |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 168h; |
Conditions | Yield |
---|---|
With pyridine at 20℃; for 20h; |
Conditions | Yield |
---|---|
With pyridine at 20℃; for 600h; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 43 percent / phenol, hydroiodic acid (d= 1.7) / 7 h / Heating 2: pyridine / 24 h View Scheme |
potassium carbonate
mangiferin
A
mangiferin-3-monopotassium
B
mangiferin-7-monopotassium
Conditions | Yield |
---|---|
In methanol; water Product distribution / selectivity; |
sodium hydrogencarbonate
mangiferin
A
mangiferin-3-monosodium
B
mangiferin-7-monosodium
Conditions | Yield |
---|---|
In ethanol; water Product distribution / selectivity; |
sodium carbonate
mangiferin
A
mangiferin-3-monosodium
B
mangiferin-7-monosodium
Conditions | Yield |
---|---|
In ethanol; water Product distribution / selectivity; |
Conditions | Yield |
---|---|
In dimethyl sulfoxide; glycerol Product distribution / selectivity; |
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