子结构搜索

241893

Fc1ccc(-c2scc(C3=CCN4CCC[C@H]4C3)c2-c2ccncc2)cc1
Reaction #9978
title compound
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69923
4-(4-methoxycarbonylthiophen-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
收率 53.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #69924
4-(4-methoxycarbonylthiophen-3-yl)-piperidine-1-carboxylic acid t-butyl ester
收率 49.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C=CC(F)=C(C)C=Cc1c(C)sc(C)c1C)=CC(N)=O
Reaction #181271
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C=Cc2ccccc2)csc1NC(=O)CC#N
Reaction #181976
DOI: 10.1039/C8SC04228D
Cc1sc(C)c2c1CCC=C2c1c[nH]cn1
Reaction #190530
DOI: 10.1039/C8SC04228D
CC1=Cc2c(sc(C)c2-c2ccc(C(C)(C)C)cc2)C1
Reaction #203355
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)sc(C)c1C
Reaction #214933
3,7-dimethyl-9-(2,4,5-trimethyl-3-thienyl)-2,4,6,8-nonatetraenoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cscc1-c1ccc(C#N)cc1C
Reaction #228732
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C=Cc2ccc(C(C)C)cc2Cl)csc1N1C(=O)c2ccccc2C1=O
Reaction #251343
DOI: 10.1039/C8SC04228D
CC(C=CC(F)=C(C)C=Cc1c(C)sc(C)c1C)=CC(=O)O
Reaction #269100
DOI: 10.1039/C8SC04228D
CC(C=CC(F)=C(C)C=Cc1c(C)sc(C)c1C)=CC(N)=O
Reaction #288438
DOI: 10.1039/C8SC04228D
CC(/C=C/c1c(C)sc(C)c1C)=C(F)\C=C\C(C)=C\C(=O)O
Reaction #311435
2E,4E,6Z,8E-3,7-dimethyl-6-fluoro-9-(2,4,5-trimethyl-3-thienyl)-2,4,6,8-nonatetraenoic acid
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)/C=C(C)/C=C/C(F)=C(C)/C=C/c1c(C)sc(C)c1C
Reaction #311436
N-ethyl (2E,4E,6Z,8E)-3,7-dimethyl-6-fluoro-9-(2,4,5-trimethyl-3-thienyl)-2,4,6,8-nonatetraenamide
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(/C=C/c1c(C)sc(C)c1C)=C(F)\C=C\C(C)=C\C(N)=O
Reaction #311437
2E,4E,6Z,8E-3,7-dimethyl-6-fluoro-9-(2,4,5-trimethyl-3-thienyl)-2,4,6,8-nonatetraenamide
收率 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(/C=C/c1c(C)sc(C)c1C)=C(F)\C=C\C(C)=C\CO
Reaction #311438
2E,4E,6Z,8E-3,7-dimethyl-6-fluoro-9-(2,4,5-trimethyl-3-thienyl)-2,4,6,8-nonatetraen-1-ol
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COC/C=C(C)/C=C/C(F)=C(C)/C=C/c1c(C)sc(C)c1C
Reaction #311439
2E,4E,6Z,8E-3,7-dimethyl-6-fluoro-9-(2,4,5-trimethyl-3-thienyl)-1-methoxy-2,4,6,8-nonatetraene
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(F)=C(C)\C=C\c1c(C)sc(C)c1C
Reaction #311444
ethyl (2E,4E)-2-fluoro-3-methyl-5-(2,4,5-trimethyl-3-thienyl)-2,4-pentadienoate
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(/C=C/c1c(C)sc(C)c1C)=C(\F)CO
Reaction #311445
2E,4E-2-fluoro-3-methyl-5-(2,4,5-trimethyl-3-thienyl)-2,4-pentadien-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(/C=C/c1c(C)sc(C)c1C)=C(\F)C=O
Reaction #311446
2E,4E-2-fluoro-3-methyl-5-(2,4,5-trimethyl-3-thienyl)-2,4-pentadien-1-al
DOI: 10.6084/m9.figshare.5104873.v1
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