Substructure Search

CCC(O)O

COc1cncc(N2CCC3(CC2)OCCO3)c1
Reaction #550
Yield 75.1%
COc1c(NC2CCC3(CC2)OCC(C)(C)CO3)ccnc1C
Reaction #1100
4-(3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-ylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C)cc(=O)n(CCC3(C#N)CCC4(CC3)OCCO4)c2c1
Reaction #67987
8-(2-(7-methoxy-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)ethyl)-1,4-dioxaspiro[4.5]decane-8-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1OC(COCc2ccc(OC)cc2)(COCc2ccc(OC)cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87465
product
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1OC(COCc2ccc(OC)cc2)(COCc2ccc(OC)cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #87485
product
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90570
307
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)C(C(OC)OC)[C@H]1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(Br)ccc2F)CO1
Reaction #155608
product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(Br)ccc3F)CO2)cn1
Reaction #155609
(4aR,6R,8aS)-8a-(5-bromo-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
OCCn1cc(-c2ccc3ncc(Cc4c(F)cc5ncccc5c4F)n3n2)cn1
Reaction #156391
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2ncccc2c(F)c1Cc1cnc2ccc(-c3cnn(CCOC4CCCCO4)c3)nn12
Reaction #156392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc2ncn(C)c2c1)c1cnc2ccc(-c3cnn(CCO)c3)nn12
Reaction #156410
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc2ncn(C)c2c1)c1cnc2ccc(-c3cnn(CCOC4CCCCO4)c3)nn12
Reaction #156411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc2nn(CCOC3CCCCO3)cc2c1)c1cnc2ccc(-c3cnn(C)c3)nn12
Reaction #156458
6-(1-methyl-1H-pyrazol-4-yl)-3-((S)-1-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-2H-indazol-5-yl}-ethyl)imidazo[1,2-b]pyridazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1cc2cnn(C)c2cc1F)c1cnc2ccc(-c3cnn(CCO)c3)nn12
Reaction #156464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2cc(Cc3cnc4ccc(-c5cnn(CCO)c5)nn34)c(F)cc21
Reaction #156465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2cc(Cc3cnc4ccc(-c5cnn(CCOC6CCCCO6)c5)nn34)c(F)cc21
Reaction #156466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2c(F)c(Cc3cnc4ccc(-c5cnn(CCO)c5)nn34)c(F)cc21
Reaction #156470
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)cc1C=O
Reaction #159767
2-Methoxy-5-((3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-benzaldehyde
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
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