部分構造検索

COCCCCI

C[C@@H](C(=O)OC(C)(C)C)N1CCC(N=[N+]=[N-])C1=O
Reaction #7373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC1CCOCC1)c1ccc2c(c1)N(C)c1ccccc1S2(=O)=O
Reaction #43265
Ethyl 2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(NC(=O)C(C[C@H]3CCC(=O)C3)c3ccc4c(c3)N(C)c3ccccc3S4(=O)=O)sc2n1
Reaction #43271
N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-((R)-3-oxocyclopentyl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(F)CCN(CC2(C(=O)OCc3ccccc3)CCOCC2)CC1
Reaction #44888
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(N)=O)c(C)c(I)c1Br
Reaction #45571
compound
収率 50.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(CI)CI
Reaction #47711
ethyl-3-iodomethyl-4-iodobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]([C@H](O)c1ccccc1)N(C)C(=O)[C@H](C[C@H]1CCC2(C1)O[C@@H](c1ccccc1)[C@H](c1ccccc1)O2)c1ccc(SC2CC2)cc1
Reaction #48245
2(R)-(4-cyclopropylsulfanylphenyl)-3-(2(S),3(S)-diphenyl-1,4-dioxaspiro[4.4]non-7(R)-yl)-N-(2(R)-hydroxy-1(R)-methyl-2-phenylethyl)-N-methylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
COCCCCC(C)(C)C(=O)OC
Reaction #50699
methyl 2,2-dimethyl-6-methoxycaproate
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c1c3cc(F)ccc3[nH]c1c1c2c2cc(F)ccc2n1[C@@H]1O[C@H](CI)C[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #52144
3,9-difluoro-12-(2,3-di-O-benzyl-4,6-dideoxy-6-iodo-β-D-glucopyranosyl)-6,7,12,13-tetrahydro(5H)indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7-dione
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC(CCCI)OC(C)=O
Reaction #54886
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
収率 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
収率 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC(CCCI)OC(C)=O
Reaction #75253
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(F)(F)CCC(F)(F)F
Reaction #76283
product
収率 76.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CCCCCCC(=O)O)S(C)(=O)=O
Reaction #93914
title compound
収率 129.3%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc([C@H]2OC3(CC[C@H](CSc4nnnn4-c4ccccc4)C3)O[C@@H]2c2ccccc2)cc1
Reaction #157700
5-({[(2R,3R,7S)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]methyl}sulfanyl)-1-phenyl-1H-tetrazole
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)c2c(Nc3ccccc3)nn(CC3CCOCC3)c2N2C1=N[C@@H]1CCC[C@@H]12
Reaction #159876
(6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-1-((tetrahydro-2H-pyran-4-yl)methyl)-cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1CC1CCOCC1
Reaction #165681
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)ccc2n1C1CCN(CC2COC(c3ccc(F)cc3)C2)CC1
Reaction #179451
DOI: 10.1039/C8SC04228D
COCCCCOC(c1ccccc1)C1CCN(C(=O)OC(C)(C)C)C1
Reaction #180567
DOI: 10.1039/C8SC04228D
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