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BrCC1CC1

COc1cccc([C@]23CCN(CC4CC4)C[C@@H]2CCC(=O)C3)c1.Cl
Reaction #2953
title compound
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(CC2CC2)c2cc(-n3cccc3)c(F)cc2c1=O
Reaction #4658
solid
Выход 62.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCOCC2CC2)ccc1OCC1CO1
Reaction #5113
2-methyl-1-(2,3-epoxypropoxy)-4-(2-(cyclopropylmethoxy)ethoxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cc2c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)nn(CC3CC3)c2C)cc1
Reaction #7488
1-(cyclopropylmethyl)-3-(β-D-glucopyranosyloxy)-5-methyl-4-[(4methylthiophenyl)methyl]-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2ccc(OC(C)C)cc2)c(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)nn1CC1CC1
Reaction #7490
1-(cyclopropylmethyl)-3-(β-D-glucopyranosyloxy)-4-[(4-isopropoxyphenyl)methyl]-5-methyl-1H-pyrazole
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(CC1CC1)C(=O)OCc1ccc(OC)cc1
Reaction #8873
title compound
Выход 60.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#Cc2cn(CC3CC3)c(C)n2)ccn1
Reaction #8961
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C#Cc2ccnc(Cl)c2)cn1CC1CC1
Reaction #8966
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)C(=O)OC(C)(C)C)c(SC)nn12
Reaction #9304
tert-butyl N-cyclopropylmethyl-N-[7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CCO3)c(SC)nn12
Reaction #9310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc(F)c(F)cc2n(CC2CC2)c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10410
title compound
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(COCC4CC4)nc3N21
Reaction #12021
compound
Выход 67.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(OCC1CC1)c1ccc2c(n1)N1[C@@H](CNC[C@H]1C)C2
Reaction #12054
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(OCC1CC1)c1ccc2c(n1)N1[C@@H](CNC[C@H]1C)C2
Reaction #12055
product
DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)N=CN(CC2CC2)c2ccc(Cl)cc21
Reaction #46123
7-chloro-4-cyclopropylmethyl-4H-1,2,4-benzothiadiazine 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1([n+]2cn(N)cn2)CC1.[Br-]
Reaction #48536
1-methylcyclopropyl-4-amino-1,2,4-triazolium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cccc(OCC2CC2)c1)[C@@H]1OC(=O)N2[C@@H]1CO[C@@H](OCC(C)(C)C)[C@@H]2C
Reaction #48746
desired compound
Выход 85.9%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCN(CC3CC3)C(Cc3ccc(O)cc31)C2=O
Reaction #54557
1,2,3,4,5,6-hexahydro-3-cyclopropylmethyl-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@]23CCCC[C@@H]2C(=O)N(CC2CC2)C(=O)C3)c1
Reaction #54753
N-Cyclopropylmethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc2cccc(OCC3CC3)c2c1C
Reaction #57576
4-cyclopropylmethoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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