Поиск подструктуры

OC1CCCCC1c1ccccc1

Cc1cc(C23CC(C)(C)CC(C)(C)C2O3)ccc1F
Reaction #6614
2-(4-fluoro-3-methylphenyl)-4,4,6,6-tetramethyl-1-epoxycyclohexane
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2CC(C)(C)CC(C)(C)C2=O)ccc1F
Reaction #6615
2-(4-fluoro-3-methylphenyl)-4,4,6,6-tetramethylcyclohexanone
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=C(C#C[Si](C)(C)C)C(C)(C)CC(C)(C)C2)ccc1F
Reaction #6616
1-((trimethylsilyl)ethynyl)-2-(4-fluoro-3-methylphenyl)-4,4,6,6-tetramethylcyclohexene
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314.C[C@H](N)C(=O)N1CCC[C@H]1C(=O)O
Reaction #60610
solid
Выход 675.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)O.COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314
Reaction #60611
solid
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)CNC(=O)CN)C(=O)O.COc1ccc2c3c1O[C@H]1C(=O)CC[C@H]4[C@@H](C2)N(C)CC[C@]314
Reaction #60612
solid
Выход 97.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(O)CC(C)(C)C2CN(C(=O)Cc3c[nH]c4ccccc34)CC21
Reaction #83691
(3aRS,4RS,5RS,7aRS)-7,7-dimethyl-4-(2-methoxyphenyl)-2-[(3-indolyl)acetyl]-4,5-perhydroisoindolediol
Выход 70.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(O)CC(C)(c2ccccc2)C2CN(Cc3ccccc3)CC21
Reaction #83717
(3aRS,4RS,5RS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-(2-methoxyphenyl)-4,5-perhydroisoindolediol
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@@]3(O)[C@H]1C5.CCC(=O)N(c1ccccc1)C1CCN(CCc2ccccc2)CC1
Reaction #155376
Naloxone Fentanyl
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2C(=O)CC[C@@]3(O)[C@H]1C5.CCC(=O)N(c1ccccc1)C1CCN(CCc2ccccc2)CC1
Reaction #155377
Naloxone Fentanyl
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC1(c2ccccc2)CCCCC12OCCO2
Reaction #158433
Methyl 4-(6-phenyl-1,4-dioxaspiro[4.5]decan-6-yl)butanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC1(c2ccccc2)CCCCC12OCCO2
Reaction #158434
residue
Выход 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2noc(CCCC3(c4ccccc4)CCCCC34OCCO4)n2)cc(C)c1OC[C@@H]1COC(C)(C)O1
Reaction #158435
3-(4-(((R)-2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-3,5-dimethylphenyl)-5-(3-(6-phenyl-1,4-dioxaspiro[4.5]decan-6-yl)propyl)-1,2,4-oxadiazole
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1CC(=O)C1NCC2C1C(c1ccccc1)(c1ccccc1)CC(O)C2(O)c1ccccc1OC
Reaction #174691
DOI: 10.1039/C8SC04228D
Cc1ncccc1NC(=O)c1ccc2c(c1)CCC1CC(O)(c3ccccc3)C(C)(O)CC21Cc1ccccc1
Reaction #177304
DOI: 10.1039/C8SC04228D
C=CCN1CCC23c4c5ccc(O)c4OC2C(=NO)CCC3(O)C1C5
Reaction #184980
DOI: 10.1039/C8SC04228D
CCOC(=O)C1C(CN)CCC(OC(C)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C1c1ccc(F)cc1
Reaction #187135
DOI: 10.1039/C8SC04228D
Oc1ccc2c(c1)C13CCCCC1(O)C(C2)NCC3
Reaction #199871
DOI: 10.1039/C8SC04228D
Cc1ccccc1C1C(OC(COC(=O)c2ccccc2)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CCC2CN(C3=NC(=O)CO3)CC21
Reaction #203904
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(C)CC2OC)C(O)C(=O)N2CCCCC2C(=O)OC(C(C)=CC2CCC(c3ccc4ccccc4c3)C(OC)C2)C(C)C(O)CC1=O
Reaction #211644
DOI: 10.1039/C8SC04228D
Страница 1Далее