NewCan Biotech Limited was established in 2021 and is primarily engaged in the research, development, production, and sales of sugars, nucleosides, nucleotides, phosphorylated monomers, as well as next-generation antiviral and antitumor drug intermed
Cas:96761-00-1
Min.Order:1 Milligram
Negotiable
Type:Trading Company
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
home-produced Application:medicine
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:96761-00-1
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryTopbatt Chemical Co., Ltd., Established in 2019, located in Shenzhen, Guangdong Province, is a Manufacturer and Trading company which specialized in fine chemicals like Pharmaceutical Reference Standards and Stable Isotopes. Our Stable Isotopes produ
1. Our staff are all biomedical related majors with rich experience in the pharmaceutical industry, and can provide you with more professional services.2. Our supplier has a good quality management system, and the quality of products is reliable and
High purity Application:Pharmaceutical intermediates, Material synthesis and analyzing the expectant ingredients
(2R,3S)-2-Triisopropylsilanyloxymethyl-2,3-dihydro-furan-3-ol
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.0166667h; | 98% |
thymidine
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With ammonium sulfate; 1,1,1,3,3,3-hexamethyl-disilazane for 4h; Heating; | 80% |
Stage #1: thymidine With ammonium sulfate; 1,1,1,3,3-pentamethyldisilazane for 2h; Reflux; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 3h; | 56% |
Stage #1: thymidine With ammonium sulfate; 1,1,1,3,3,3-hexamethyl-disilazane at 130℃; for 2h; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 3h; | 50% |
2,3-O-Isopropylidene-5-O-trityl-α,β-ribofuranosyl chloride
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With ammonia; lithium In tetrahydrofuran for 2h; |
2'-Deoxyguanosine
17β-Estradiol-3,4-quinone
A
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With acetic acid In water; N,N-dimethyl-formamide at 22℃; pH=4.0; Product distribution; |
2'-Deoxyguanosine
hexestrol-3',4'-quinone
A
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With acetic acid In water; N,N-dimethyl-formamide at 22℃; pH=4.0; Product distribution; |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane
1,4-anhydro-2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide | 80% |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
8-iodo-2-methyl-4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-4-one
2-methyl-4-(N-methyl-N-phenylamino)-8-(β-D-glycero-pentofuran-3'-ulose-1'-yl)pyrazolo[1,5-a]-1,3,5-triazine
Conditions | Yield |
---|---|
With tributyl-amine; triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0) In acetonitrile at 60℃; for 18h; | 75% |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With tributyl-amine; triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0) In N,N-dimethyl-formamide at 100℃; Heck Reaction; Inert atmosphere; regioselective reaction; | 60% |
8-iodo-4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazine
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
With triphenyl-arsane; triethylamine; bis(dibenzylideneacetone)-palladium(0) In acetonitrile at 100℃; for 16h; Solvent; Reagent/catalyst; | 34% |
With tributyl-amine; triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0) In acetonitrile at 60℃; for 12.25h; | |
With triphenyl-arsane; triethylamine; bis(dibenzylideneacetone)-palladium(0) In acetonitrile at 82℃; for 16h; |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
8-(2'-deoxy-β-D-ribofuranosyl)-2-methyl-4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / bis(dibenzylideneacetone)palladium(0); Ph3As; (n-Bu)3N / acetonitrile / 18 h / 60 °C 2: 92 percent / sodium triacetoxyborohydride / acetonitrile / 0.33 h / 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
8-(2'-deoxy-β-D-xylofuranosyl)-2-methyl-4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / bis(dibenzylideneacetone)palladium(0); Ph3As; (n-Bu)3N / acetonitrile / 18 h / 60 °C 2: 78 percent / K-selectride / acetonitrile / 0.33 h / 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
8-(2'-deoxy-β-D-xylofuranosyl)-2-methyl-4-(N-methylamino)pyrazolo[1,5-a]-1,3,5-triazine 3',5'-cyclic phosphate benzyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 75 percent / bis(dibenzylideneacetone)palladium(0); Ph3As; (n-Bu)3N / acetonitrile / 18 h / 60 °C 2: 78 percent / K-selectride / acetonitrile / 0.33 h / 20 °C 3: 67 percent / ethanol / 12 h / 100 °C 4: 63 percent / t-BuOK / tetrahydrofuran / -40 - 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 75 percent / bis(dibenzylideneacetone)palladium(0); Ph3As; (n-Bu)3N / acetonitrile / 18 h / 60 °C 2: 92 percent / sodium triacetoxyborohydride / acetonitrile / 0.33 h / 20 °C 3: 73 percent / ethanol / 12 h / 100 °C 4: 66 percent / t-BuOK / tetrahydrofuran / -40 - 20 °C 5: 91 percent / H2 / Pd/C / methanol / 1.4 h / 20 °C / 3102.97 Torr View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
8-(2'-deoxy-β-D-ribofuranosyl)-2-methyl-4-(N-methylamino)pyrazolo[1,5-a]-1,3,5-triazine 3',5'-bis(dibenzyl phosphate)
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 75 percent / bis(dibenzylideneacetone)palladium(0); Ph3As; (n-Bu)3N / acetonitrile / 18 h / 60 °C 2: 92 percent / sodium triacetoxyborohydride / acetonitrile / 0.33 h / 20 °C 3: 73 percent / ethanol / 12 h / 100 °C 4: 66 percent / t-BuOK / tetrahydrofuran / -40 - 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
(2R,3S)-3-(benzyloxy)-2-((benzyloxy)methyl)-2,3-dihydrofuran
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine / 1 h / Ambient temperature 2: 91 percent / NaOH, K2CO3 / dimethylsulfoxide / 2 h / Ambient temperature View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
1,3-Dimethyl-2'-deoxypseudouridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) Pd(OAc)2, 2.) Na2CO3 / 1.) acetonitrile, RT, 42 h, 2.) acetonitrile, 65 deg C, 1 h 2: 21 percent / LiBH4 / tetrahydrofuran / 1.5 h / -78 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
5-(2'-deoxy-β-D-threo-pentofuranosyl)-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) Pd(OAc)2, 2.) Na2CO3 / 1.) acetonitrile, RT, 42 h, 2.) acetonitrile, 65 deg C, 1 h 2: 40 percent / LiBH4 / tetrahydrofuran / 1.5 h / -78 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube View Scheme | |
Multi-step reaction with 4 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2.1: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3.1: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4.1: ammonia / methanol / 19 h / 100 °C / Sealed tube 5.1: pyridine / 2 h / 0 - 20 °C 5.2: 0.83 h / 0 - 20 °C View Scheme | |
Multi-step reaction with 5 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube 5: pyridine / 2.5 h / 0 - 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2.1: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3.1: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4.1: ammonia / methanol / 19 h / 100 °C / Sealed tube 5.1: pyridine / 2 h / 0 - 20 °C 5.2: 0.83 h / 0 - 20 °C 6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C View Scheme | |
Multi-step reaction with 6 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube 5: pyridine / 2.5 h / 0 - 20 °C 6: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2.1: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3.1: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4.1: ammonia / methanol / 19 h / 100 °C / Sealed tube 5.1: pyridine / 2 h / 0 - 20 °C 5.2: 0.83 h / 0 - 20 °C 6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C 7.1: pyridine / 19 h / 0 - 20 °C View Scheme | |
Multi-step reaction with 7 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube 5: pyridine / 2.5 h / 0 - 20 °C 6: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C 7: pyridine / 19 h / 0 - 20 °C / Inert atmosphere View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2.1: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3.1: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4.1: ammonia / methanol / 19 h / 100 °C / Sealed tube 5.1: pyridine / 2 h / 0 - 20 °C 5.2: 0.83 h / 0 - 20 °C 6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C 7.1: pyridine / 19 h / 0 - 20 °C 8.1: DCI / dichloromethane / 1 h / 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 8 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C 3: 1H-imidazole / N,N-dimethyl-formamide / 60 h / 20 °C 4: ammonia / methanol / 19 h / 100 °C / Sealed tube 5: pyridine / 2.5 h / 0 - 20 °C 6: tetrabutyl ammonium fluoride / tetrahydrofuran / 6 h / 20 °C 7: pyridine / 19 h / 0 - 20 °C / Inert atmosphere 8: 4,5-dicyano-1H-imidazole / acetonitrile; dichloromethane / 1 h / 20 °C / Inert atmosphere View Scheme |
1,4-anhydro-2-deoxy-D-erythro-pent-1-enitol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triphenyl-arsane; bis(dibenzylideneacetone)-palladium(0); triethylamine / acetonitrile / 16 h / 82 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: triethylamine; bis(dibenzylideneacetone)-palladium(0); triphenyl-arsane / acetonitrile / 16 h / 100 °C 2: sodium tris(acetoxy)borohydride / acetonitrile / 5 h / 20 °C View Scheme |
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