Поиск подструктуры

339540

CCCCCCCCCCCCCCC(O)(CCCCCCCCCC)CCCCCCCCCC
Reaction #2684
di-n-decyl-n-tetradecylcarbinol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCC(O)(CCCCCCCCCC)CCCCCCCCCCCCCC
Reaction #2686
n-nonadecyl-n-tetradecyl-n-decylcarbinol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(=O)C1([C@H]2CC[C@H](OC3CCCCO3)CC2)C=CC(c2ccccc2)=CC1
Reaction #5400
trans-4-(4-decanoyl-4-biphenylyl)cyclohexyl tetrahydropyranyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC1CCCC1)[C@H](O)CO
Reaction #42553
tert-butyl (1S,2S)-1-[cyclopentylmethy]-2,3-dihydroxypropylcarbamate
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)(/C=C/[C@H]1CCC(=O)N1CCSCCCC(=O)O)CCCCC
Reaction #51254
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCCC
Reaction #52077
6-undecanol
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1C(=O)C1CCCC1
Reaction #58586
crude product
Выход 93.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCc1ccsc1
Reaction #77176
3-n-octadecylthiophene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(O)c1cccc(C(=O)OC)c1
Reaction #87303
methyl (RS)-3-[1-hydroxyoctyl]benzoate
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H]2O[C@H](C(O)C3CCCC3)C[C@H]2O1
Reaction #88981
crude product
Выход 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(O)CC(O)CCCCCC
Reaction #157937
desired product
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C2CCCC2)c(C(F)(F)F)c1
Reaction #304653
4-cyclopentyl-3-(trifluoromethyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCn2c(C(F)(F)F)nc(C(=O)C3CCCC3)c2C1
Reaction #308667
1-cyclopentanecarbonyl-3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazine-7-carboxylic acid tert-butyl ester
Выход 32.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)Cc1c(-c2ccc(C)cc2)nc2ccc(C)cn12
Reaction #317432
1-(6-Methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-heptan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
C(CCCCCCC1CCCCC1)CCCCCOC1CCCCO1
Reaction #318447
[(12-cyclohexyldodecyl)oxy]-tetrahydro-2H-pyran
DOI: 10.6084/m9.figshare.5104873.v1
[Br][Mg][CH2]C1CCCCC1
Reaction #321667
cyclohexylmethylmagnesium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1C(=O)C1CCCCC1
Reaction #322421
(2-acetamidophenyl) cyclohexyl methanone
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1cc(C)ccn1
Reaction #328662
product
Выход 44.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1cc(C)ccn1
Reaction #328664
4-methyl-2-hexyl-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1cc(CC)ccn1
Reaction #328665
4-ethyl-2-hexyl-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее