Recherche de Sous-structure

678243

CC(C)C(C)([NH-])C(N)=O.CCOC(=O)/C(C)=C(\C)C(=O)[O-]
Reaction #4225
monoethyl-2,3-dimethylfumarate N-(1-aminocarbonyl-1-methylisobutyl)-amide
Rendement 42.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Cc2cccc(OC)c2C1C(=O)OCC
Reaction #5441
desired product
Rendement 96.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCCCC(=CC(=O)OC(C)(C)C)C(=O)N1
Reaction #5501
ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #5502
ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(C)C=CC(=O)c1cc(OC)ccc1OCC(C)C
Reaction #44923
ethyl 6-(2-isobutoxy-5-methoxyphenyl)-6-oxo-3-methylhexa-2,4-dienoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCCCC(=CC(=O)OC(C)(C)C)C(=O)N1
Reaction #50256
ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #50257
ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2S(=O)C1
Reaction #54319
benzhydryl 7-phenoxyacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate-1-oxide
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1
C[NH-]
Reaction #183557
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C(=O)OCC)c1ccc2nc(C)ccc2c1
Reaction #198603
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C(=O)OCC)c1ccc(C)cc1
Reaction #199013
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1C(=O)N2C(C(=O)OC(C)(C)C)=C(C=O)CCC12
Reaction #210029
DOI: 10.1039/C8SC04228D
CCCCOC(=O)/C=C(/C)C=O
Reaction #214929
3-formyl-crotonic acid butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C=C(C)C=CC=C(C)C=O
Reaction #214932
7-formyl-3-methyl-octa-2,4,6-trien-1-oic acid butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\C)C(O)CC(=O)c1cc2c(cc1C)C(C)(C)CCC2(C)C
Reaction #216440
alcohol
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1CN(C(c2ccccc2)(c2ccccc2)c2ccccc2)CCC1O
Reaction #231362
DOI: 10.1039/C8SC04228D
Nc1nc(C(=NOC(c2ccccc2)(c2ccccc2)c2ccccc2)C(=O)NC2C(=O)N3C(C(=O)OC(c4ccccc4)c4ccccc4)=C(C=O)CSC23)ns1
Reaction #240005
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC1(C(=O)OCC)c1ccc2nc(C)ccc2c1
Reaction #278571
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCCCCCC(=CC(=O)OC(C)(C)C)C(=O)N1
Reaction #280971
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC1(C(=O)OCC)c1cccc2ncccc12
Reaction #291711
DOI: 10.1039/C8SC04228D
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