子结构搜索

10319

CCOC(=O)c1c2c(c(C(O)(c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2691
Bis-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole-4-yl)-mono-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(C(c3c4c(c(C(=O)OC)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)OC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2695
Bis-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis (1,3) dioxol-4-yl)-mono-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methane
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2c(c(C(O)(c3c4c(c(C(=O)N(CCO)CCO)c5c3SC(C)(C)O5)OC(C)(C)S4)c3c4c(c(C(=O)N(CCO)CCO)c5c3SC(C)(C)O5)OC(C)(C)S4)c3c(c2C(=O)N(CCO)CCO)OC(C)(C)S3)S1
Reaction #2699
amide
收率 63.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(=O)c(O)c2c(O)c(O)cc([C@H]3Oc4cc(O)cc(O)c4C[C@H]3OC(=O)c3cc(O)c(O)c(O)c3)c2c1)c1cc(O)c(O)c(O)c1
Reaction #8612
theaflavin 3,3′-digallate
收率 10.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(=O)c(O)c2c(O)c(O)cc([C@@H]3Oc4cc(O)cc(O)c4C[C@@H]3O)c2c1)c1cc(O)c(O)c(O)c1
Reaction #8616
compound 3
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(O)ccc2c1OCCO2
Reaction #66663
5-isopropyl-6 hydroxy-2,3-dihydro-benzo[1,4]dioxine
收率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2COc3ccc4c(c3O2)CCO4)cc1
Reaction #77530
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C1=C(c2c[nH]c3ccccc23)CCN(CC2COc3ccc4c(c3O2)CCO4)C1
Reaction #77531
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2COc3ccc4occc4c3O2)cc1
Reaction #77532
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2COc3ccc4c(c3O2)CCCO4)cc1
Reaction #77535
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2[nH]cc(C3=CCN(CC4COc5ccc6c(c5O4)CCCO6)CC3)c2c1
Reaction #77536
desired product
收率 53.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(N3CCCN(c4ccc(-c5cc(OC)c(C)c(OC)c5)cn4)CC3)nc2)cc(OC)c1C.CS(=O)(=O)O.CS(=O)(=O)O
Reaction #77586
title compound
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(/C=C/S(=O)Cc2cnc(OC)c([N+](=O)[O-])c2)c(OC)c1
Reaction #159840
(E)-2-methoxy-3-nitro-5-((2,4,6-trimethoxystyrylsulfinyl)methyl)pyridine
收率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(O)ccc2c1OCCO2
Reaction #168984
5-isopropyl-6 hydroxy-2,3-dihydro-benzo[1,4]dioxine
收率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(NC(=O)c2cc(Oc3ccc(C(=N)NO)nc3)c3c(c2)OC(C)(C)C3)n1
Reaction #175138
DOI: 10.1039/C8SC04228D
CC(C)c1c(O)ccc2c1OCCO2
Reaction #177306
DOI: 10.1039/C8SC04228D
COCC1Cc2c(Oc3ccc(C(=O)N4CCC4)cc3)cc(C(=O)Nc3ccn(C)n3)cc2O1
Reaction #192971
DOI: 10.1039/C8SC04228D
CCCc1c(OCCCCCC(=O)NCCCCOc2cccnc2)ccc(C(C)=O)c1O
Reaction #199129
DOI: 10.1039/C8SC04228D
COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)C(=O)OC(C)(C)C)c(COC)nn23)c(OC)c1
Reaction #199257
DOI: 10.1039/C8SC04228D
Cn1ccc(NC(=O)c2cc(Oc3cc(F)cc(F)c3)c3c(c2)OC(C)(C)C3)n1
Reaction #205342
DOI: 10.1039/C8SC04228D
第 1 页下一页