m ch 55 Search Results


fetal bovine serum  (ATCC)
95
ATCC fetal bovine serum
Fetal Bovine Serum, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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m ch 55  (Tocris)
94
Tocris m ch 55
M Ch 55, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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sativa l ch m herb ishpit  (Medicago)
90
Medicago sativa l ch m herb ishpit
Sativa L Ch M Herb Ishpit, supplied by Medicago, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cholinesterase inhibitor tacrine hydrochloride  (Tocris)
90
Tocris cholinesterase inhibitor tacrine hydrochloride
Cholinesterase Inhibitor Tacrine Hydrochloride, supplied by Tocris, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cosmosil 5c18-arii  (Nacalai)
90
Nacalai cosmosil 5c18-arii
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Cosmosil 5c18 Arii, supplied by Nacalai, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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amadori compounds  (British Poultry Science Ltd)
90
British Poultry Science Ltd amadori compounds
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Amadori Compounds, supplied by British Poultry Science Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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apparatus coess 1998  (Informa UK Limited)
90
Informa UK Limited apparatus coess 1998
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Apparatus Coess 1998, supplied by Informa UK Limited, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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apparatus coess 1998 - by Bioz Stars, 2026-03
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m csf  (Bio-Techne corporation)
99
Bio-Techne corporation m csf
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
M Csf, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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beyoecl plus assay kit  (Beyotime)
90
Beyotime beyoecl plus assay kit
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Beyoecl Plus Assay Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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beyoecl plus assay kit - by Bioz Stars, 2026-03
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ch 2 01  (Bio-Rad)
91
Bio-Rad ch 2 01
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Ch 2 01, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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jlc-300 amino acid analyzer  (JEOL)
90
JEOL jlc-300 amino acid analyzer
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
Jlc 300 Amino Acid Analyzer, supplied by JEOL, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
jlc-300 amino acid analyzer - by Bioz Stars, 2026-03
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8i m serrano lab  (Bio-Techne corporation)
92
Bio-Techne corporation 8i m serrano lab
Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, <t>HPLC</t> <t>purification,</t> and then 5% acetic acid.
8i M Serrano Lab, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, HPLC purification, and then 5% acetic acid.

Journal: RSC Advances

Article Title: Design and synthesis of purine nucleoside analogues for the formation of stable anti-parallel-type triplex DNA with duplex DNA bearing the 5m CG base pair †

doi: 10.1039/d1ra02831f

Figure Lengend Snippet: Synthesis of amidite compounds of new nucleoside analogues and TFOs. Reagents and conditions: (a) DMTrCl, pyridine, 92%, (b) (1) ethylenediamine, EtOH, 60 °C, (2) FmocCl, Et 3 N, CH 2 Cl 2 , 57% in 2 steps, (c) TBSCl, imidazole, CH 3 CN, 86%, (d) (1) PdAc 2 , xantphos, toluene, 3-aminophenyl benzoate, Cs 2 CO 3 , (2) Et 3 N–3HF, Et 3 N, THF, 80% in two steps, (e) (1) PdAc 2 , xantphos, toluene, 2-aminophenyl benzoate, NaO t Bu, (2) Bz 2 O, DMAP, (3) Et 3 N–3HF, Et 3 N, THF, 35% in three steps, (f) 2-cyanoethyl- N , N -diisopropylchlorophosphoramidite, DIPEA, CH 2 CH 2 , 0 °C, 49, 63, or 66% for 10, 11, or 12, respectively, (g) DNA automated synthesizer, followed by 28% ammonia solution at 55 °C for 12 h, HPLC purification, and then 5% acetic acid.

Article Snippet: Cleavage from the resin was accomplished by an overnight treatment with 28% ammonium hydroxide at 55 °C for 5 h, followed by reversed-phase HPLC purification (column: Nacalai Tesque COSMOSIL 5C18-ARII, 10 × 250 mm, solvents: A: 0.1 M TEAA buffer, B: CH 3 CN, gradient: B for 10% to 40%/20 min, flow rate: 3.0 mL min −1 , UV: 254 nm, column oven: 35 °C).

Techniques: Analogues, Purification