Recherche de Sous-structure

C1CO1

CCCCCCCCCCCCCCOCC(O)CNCCCO
Reaction #1200
title compound
Rendement 135.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCOCC(C)(O)CCNCCO
Reaction #1201
title compound
Rendement 30.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOCC(O)CNCCOP(=O)([O-])O.[Na+]
Reaction #1202
title compound
Rendement 36.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1205
title compound
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CN
Reaction #1218
title compound
Rendement 83.1%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(OCc2ccccc2)c1C[C@H]1CO1
Reaction #1615
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(-n2nc(CCC3CO3)[nH]c2=O)c(Cl)cc1Cl
Reaction #2058
title compound
Rendement 95.4%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOc1cc(-n2nc3n(c2=O)CC(O)CC3)c(Cl)cc1Cl
Reaction #2059
title product
Rendement 36.8%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccccc1C1CO1
Reaction #2158
oil
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(O)(COc1ccc(Cl)cc1)Cn1cncn1
Reaction #4220
2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1yl)butan-2-ol
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1(COc2ccc(Cl)cc2)CO1
Reaction #4221
2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)C(F)(F)C(F)(F)C1(Cn2cncn2)CO1
Reaction #4819
2-heptafluoropropyl-2-(1H-1,2,4-triazol-1-ylmethyl)oxirane
Rendement 2.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCCNC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)c(C)c1
Reaction #42325
tert-butyl (1S,2R)-1-benzyl-3-{[3-(2,4-dimethylphenyl)propyl]amino}-2-hydroxypropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](CC2CCCCC2)[C@H](O)CNCc2cccc(CC)c2)c1.Cl
Reaction #42554
N1-{(1S,2R)-1-(cyclohexylmethyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-5-methyl-N3,N3-dipropylisophthalamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](CC2CCCCC2)[C@H](O)CNCc2cccc(Br)c2)c1.Cl
Reaction #42555
N1-[(1S,2R)-3-[(3-bromobenzyl)amino]-1-(cyclohexylmethyl)-2-hydroxypropyl]-5-methyl-N3,N3-dipropylisophthalamide hydrochloride
Rendement 38.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@H]1CO1
Reaction #48320
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@H](O)COC(C)=O
Reaction #48321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CN[C@H]1CC(C)(C(F)(F)F)Oc2ccc(Br)cc21
Reaction #48336
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](O[Si](CC)(CC)CC)[C@@H](C)[C@H](O)[C@H](C)C=O
Reaction #50360
31
DOI: 10.6084/m9.figshare.5104873.v1
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