部分構造検索

CC(O)OC

COC(=O)C(CN1C(=O)c2c(F)ccc(F)c2C1=O)C1(C)OCCO1
Reaction #10935
Methyl 3-(4,7-difluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C1(C)OCCO1
Reaction #10959
Ethyl 3-(1,3-dioxo-1,3,4,5,6,7-hexahydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C(C)=O
Reaction #10980
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN(C(c2ccc(Cl)cc2)c2ccc(C=O)cc2)C1)c1cc(F)cc(F)c1
Reaction #53471
(−)-1-[(4-chlorophenyl)(4-formylphenyl)methyl]-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
収率 105.1%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCCNC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #66333
N-Fmoc-4-amino-butyraldehyde
収率 98000.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCCNC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #66400
N-Fmoc-4-amino-butyraldehyde
収率 98000.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)CCC(COC1CCCCO1)C2
Reaction #82233
methyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylate
収率 99.3%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
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OCCO)cc3)cn(CC(=O)OCC)c12
Reaction #155348
ethyl{5-fluoro-3-[4-(2-hydroxyethoxy)phenyl]-4-oxo-8-propoxy-4H-quinolin-1-yl}acetate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CCCCNC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #155401
N-Fmoc-4-amino-butyraldehyde
収率 98000.0%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
O=C(OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(=O)c3ccccc3)[C@@H](O[C@@H]3[C@H](OC(=O)c4ccccc4)[C@@H](OCc4ccccc4)O[C@H](COC(=O)c4ccccc4)[C@H]3OC(=O)c3ccccc3)O[C@H](COC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162021
trisaccharide
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H](COCc2ccccc2)O[C@@H]1O
Reaction #163504
3,4,6-tri-O-benzyl-α-D-mannose
収率 127.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1(Br)CCOC1OC
Reaction #165927
ethyl-2-(3-bromo-2-methoxytetrahydrofuran-3-yl)-2-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1(Br)CCOC1OCC
Reaction #165928
Ethyl-2-(3-bromo-2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1CCOC1OC
Reaction #165929
Ethyl-2-(2-methoxytetrahydrofuran-3-yl)-2-oxoacetate
収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1CCOC1OCC
Reaction #165930
Ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate
収率 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1OC(OCCCCCCCCCCO)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #174917
DOI: 10.1039/C8SC04228D
C#Cc1ccc(Cc2cc(C3(O)OC(CO)C(O)C(O)C3O)ccc2Cl)cc1
Reaction #181164
DOI: 10.1039/C8SC04228D
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