2-bromothiophene

COC(=O)C(O)(c1cccs1)c1cccs1
Reaction #42720
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CO[Si](OC)(c1cccs1)c1cccs1
Reaction #72405
dithienyldimethoxysilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1ccc(Cc2cccs2)cc1
Reaction #80456
2-(4-fluorobenzyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Fc1ccc(Cc2ccc(Br)s2)cc1
Reaction #80470
2-bromo-5-(4-fluorophenylmethyl)thiophene
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)CCC(=O)c1ccc(Br)s1
Reaction #94755
4-(5-bromo-2-thienyl)-4-ketobutyric acid
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C(O)CCC(=O)c1ccc(Br)s1
Reaction #94778
4-(5-bromo-2-thienyl)-4-ketobutyric acid
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
O=C(O)CCC(=O)c1ccc(Br)s1
Reaction #94801
4-(5-bromo-2-thienyl)-4-ketobutyric acid
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cc1ccncc1N1CCN(c2cccs2)C1=O
Reaction #167248
product
Ausbeute 109.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCC(=O)c1ccc(Br)s1
Reaction #177919
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C1(c2cccs2)CCN(C(=O)OC(C)(C)C)CC1
Reaction #186392
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1csc(OC2CCCC2)c1
Reaction #196678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[Si](C)(C)C#Cc1cccs1
Reaction #204634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)N(C(=O)C=Cc1cccs1)C(C)C
Reaction #210747
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(O)(c2cccs2)CC1
Reaction #225137
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1ccc(-c2ccc(-c3cccs3)c(F)c2)cc1
Reaction #237398
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=C(Br)Cc1cccs1
Reaction #247908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cccs1
Reaction #249459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-c2cccs2)cc1
Reaction #251585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1csc(-c2ccncc2)c1
Reaction #261700
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccc(Cc2cccs2)cc1
Reaction #265115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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