Поиск подструктуры

510852

CC(=O)C(O)[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(-c3ccccn3)cc2)[C@@](O)(C(C)=O)[C@](O)(C(C)=O)[C@@]1(O)C(C)=O
Reaction #7479
5-Methyl-4-{[4-(pyridin-2-yl)phenyl]methyl}-3-(2,3,4,6-tetraacetyl-β-D-glucopyranosyloxy)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73563
(2S)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one
Выход 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)[C@@](O)(C(=O)O)[C@](O)(C(=O)O)C(=O)c2ccc(C)cc2)cc1.N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73564
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane di-p-toluoyl-D-tartrate salt
Выход 58.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73565
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
Выход 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1(C)CCCC(C)(C)C12CCC(C)O2
Reaction #74884
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-6-yl acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #74885
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-3-ene-6-ol
Выход 174.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1(C)CCCC(C)(C)C12CCC(C)O2
Reaction #74886
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC1(C)CCCC(C)(C)C12CCC(C)O2
Reaction #74887
ester
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OC1(C)CCCC(C)(C)C12CCC(C)O2
Reaction #74888
ester
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC2(O1)C(C)(C)CCCC2(C)OC(=O)C(C)C
Reaction #74889
ester
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169609
(2S)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one
Выход 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)[C@@](O)(C(=O)O)[C@](O)(C(=O)O)C(=O)c2ccc(C)cc2)cc1.N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169610
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane di-p-toluoyl-D-tartrate salt
Выход 58.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169611
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
Выход 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H]2CNC(=O)c3cc(Cl)ccc3[C@H]2C1
Reaction #172134
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1(C2(c3ccc(Cl)cc3)CO2)CC1
Reaction #176358
DOI: 10.1039/C8SC04228D
Cc1ncccc1NC(=O)c1ccc2c(c1)CCC1CC(O)(c3ccccc3)C(C)(O)CC21Cc1ccccc1
Reaction #177304
DOI: 10.1039/C8SC04228D
CC1C=CC2(O1)C(C)(C)CCCC2(C)O
Reaction #184137
DOI: 10.1039/C8SC04228D
CC(C)(Oc1ccc(Cl)cc1)C(O)(Cn1cncn1)c1ccc(Cl)cc1
Reaction #192225
DOI: 10.1039/C8SC04228D
COC(=O)CCC1(C(C)(C)O[SiH2]C(C)(C)C)CC(c2ccc(OCc3cc(C)nc4ccccc34)cc2)=NO1
Reaction #202368
DOI: 10.1039/C8SC04228D
COC1OC(CO)C(O)(C(=O)c2ccccc2)C1(O)C(=O)c1ccccc1
Reaction #213225
DOI: 10.1039/C8SC04228D
Страница 1Далее