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10046

CCOP(=O)(COCCOn1cnc2c(Cl)ncnc21)OCC
Reaction #6339
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COCCOn1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #6340
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COC(COCc1ccccc1)COn1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #6343
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1nc(Cl)c2ncn(OCc3ccccc3)c2n1
Reaction #6350
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC=Nc1occ(-c2ccc(NC(C)=O)cc2)c1C#N
Reaction #60752
6
Выход 52.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nncn2c1
Reaction #88901
6-Fluoro-[1,2,4]triazolo[4,3-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(CC)(OC(=O)C(=C)C)OC(=O)C(=C)C
Reaction #322861
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COCCCOn1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #432239
6-chloro-9-[3-(diethoxyphosphorylmethoxy)propoxy]-2-formamidopurine
Выход 69.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COCC(CO[Si](C)(C)C(C)(C)C)On1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #432245
9-(1-t-Butyldimethylsilyloxy-3-diethoxyphosphorylmethoxyprop -2-oxy)-6-chloro-2-formamidopurine
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COCC(CO[Si](C)(C)C(C)(C)C)On1cnc2c(Cl)ncnc21)OCC
Reaction #432247
9-(1-t-butyldimethylsilyloxy -3-diethoxyphosphorylmethoxyprop-2-oxy)-6-chloropurine
Выход 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCOn1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #461058
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCOn1cnc2c(Cl)nc(NC=O)nc21)OCC
Reaction #461061
title compound
Выход 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCOn1cnc2c(Cl)ncnc21)OCC
Reaction #461063
title compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCOn1cnc2c(Cl)ncnc21)OCC
Reaction #461065
title compound
Выход 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCC(CO[Si](C)(C)C(C)(C)C)On1cnc2c(Cl)ncnc21)OCC
Reaction #461072
title compound
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)C(C)C(OCC)OCC
Reaction #523885
oil
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2ocnc2c1)N1CC=CCC1
Reaction #529826
1-(1,3-benzoxazol-5-ylcarbonyl)-1,2,3,6-tetrahydropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1[C@H]1CCN(C)CCN1C(=O)N(C)Cc1cc(Cl)cc(Cl)c1
Reaction #547117
7-(R)-(4-fluoro-2-methyl-phenyl)-4-methyl-[1,4]-diazepane-1-carboxylic acid, (3,5-dichloro-benzyl)-methylamide
Выход 20.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1[C@H]1CCN(C)CCN1C(=O)N(C)Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #547118
7-(R)-(4-fluoro-2-methyl-phenyl)-4-methyl-[1,4]-diazepane-1-carboxylic acid, (3,5-bis-trifluoromethyl-benzyl)-methylamide
Выход 23.6%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1nc(Cl)c2ncn(OCc3ccccc3)c2n1
Reaction #554404
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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