2-methylthiophene

Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)s1
Reaction #2704
title compound
収率 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
Reaction #2715
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)s1
Reaction #2719
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1ccc(O)c(C(=O)c2ccc(C)s2)c1
Reaction #94590
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COC(=O)C(=O)c1ccc(C)s1
Reaction #164242
oil
収率 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)NC(C)(C)C)s1
Reaction #248959
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(CCCCBr)s1
Reaction #258601
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(S(=O)(=O)NC(C)(C)C)s1
Reaction #311854
N-tert.-butyl-5-methyl-thiophene-2-sulfonamide
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
CCc1c(C)sc(S(=O)(=O)NC(C)(C)C)c1C(=O)O
Reaction #311860
4-ethyl-5-methyl-2-(N-tert.butyl) sulfamoyl-thiophene-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
Cc1ccc(B(O)O)s1
Reaction #321637
2-methylthiophene-5-boronic acid
収率 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Cc1ccc(C(=O)c2ccc(F)cc2)s1
Reaction #346075
p-fluorophenyl 5-methyl-2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
COC(=O)C(=O)c1ccc(C)s1
Reaction #385870
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(C2(O)c3ccccc3-c3ccccc32)s1
Reaction #389676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(O)c1ccc(C)s1
Reaction #446931
title compound
収率 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
COc1ccc(-c2cc(Br)c(C)s2)cc1
Reaction #473499
5-(4′-methoxyphenyl)-3-bromo-2-methylthiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(C(=O)c2ccc(F)cc2)s1
Reaction #548887
p-fluorophenyl 5-methyl-2-thienyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
Cc1cc2c(s1)C(=O)C(C)C2
Reaction #579401
product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Cc1cc2c(s1)C(=O)C(C)C2
Reaction #579402
product
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
—
Reaction #706797
EtOAc hexanes
収率 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
—
Reaction #706807
EtOAc hexanes
収率 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
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