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CC(C)CBr

CCCCC[Si@H]1CC[C@H](c2cc(F)c(C[C@@H](C)CC)c(F)c2)CC1
Reaction #2744
(S)-4-(trans-4-n-pentyl-4-silacyclohexyl)-1-(2-methylbutyl)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[Si@H]1CC[C@H]([C@H]2CC[C@H](c3ccc(C[C@@H](C)CC)cc3)CC2)CC1
Reaction #2748
(S)-4-(trans-4-(trans-4-n-pentyl-4-silacyclohexyl)cyclohexyl)-1-(2- methylbutyl) benzene
DOI: 10.6084/m9.figshare.5104873.v1
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
CC(=CC(=O)O)c1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #4840
3-methyl-3-{4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid
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
O=C1Nc2ccccc2C12CCCC2Br
Reaction #7092
subtitled compound
Выход 105.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C12CCCC2B(O)O
Reaction #7108
subtitled compound
Выход 64.0%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
COC(=O)c1cc(-c2ccc(C)c(F)c2)nn(CC(C)C)c1=O
Reaction #8007
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(-c2cc(C(=O)O)c(=O)n(CC(C)C)n2)cc1
Reaction #8089
title compound
Выход 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(CC2CCCC2)c1=O
Reaction #8098
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(C#N)cc1
Reaction #8143
4-iso-butoxybenzo-nitrile
Выход 85.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)CC(CBr)Cc1ccccc1
Reaction #8315
3-benzyl-4-bromo-butyryl chloride
Выход 127.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CBr)Cc1ccccc1)NN=C(Cc1ccnc2ccccc12)c1ccccn1
Reaction #8316
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[Si](c1ccccc1)(c1ccccc1)C1(CC(C)C)SCCCS1
Reaction #8635
26
Выход 92.5%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(CC(C)C)c(C)n2)ccn1
Reaction #8960
title compound
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
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