Участвует в 118 реакциях

1435366

O=C1c2cc(OCCCc3ccccc3)ccc2C(c2ccccc2)C1Br
Reaction #46166
title compound
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(CBr)cc2C1=O
Reaction #46172
6-bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester
Выход 36.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(CBr)cc2C1=O
Reaction #47813
titled compound
Выход 36.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1C(Br)=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc21
Reaction #47815
titled compound
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
Reaction #47824
titled compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)NS(=O)(=O)c1ccccc1-c1ccc(CBr)c(F)c1
Reaction #64576
title compound
Выход 81.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)c1nc(CBr)n(Cc2ccccc2)c1C(=O)OCC
Reaction #81324
title compound
Выход 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1c(CBr)cccc1O[Si](C)(C)C(C)(C)C
Reaction #87954
methyl 2-bromomethyl-6-(tert-butyldimethylsilyloxy)benzoate
Выход 32.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1CS(=O)(=O)OC1=O
Reaction #94709
4-METHYL-1,2-OXATHIOLANE-5-ONE-2,2-DIOXIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC(C)(C)OC(=O)C1=C(CBr)CS(=O)[C@@H]2C(NC=O)C(=O)N12
Reaction #96235
t-butyl 3-bromomethyl-7-formamido-3-cephem-4-carboxylate-1-oxide
Выход 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COC(=O)c1ccc(Br)cc1CBr
Reaction #174435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(CBr)cc1)C1CCC1
Reaction #195318
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cc(CBr)ccn1
Reaction #203101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Br)cc(CBr)c1
Reaction #203801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC1CNCC12CCC2
Reaction #231320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)N1CCOc2ccc(CBr)cc21
Reaction #235952
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1c(Cc2c(C)[nH]c3ccccc23)sc2c1c(=O)n(C)c(=O)n2CC(C)C
Reaction #247003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ncsc1CBr
Reaction #249920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)OC1CNCC12CC2
Reaction #257642
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cnnc2c(CCl)cccc12
Reaction #343048
methyl 8-(chloromethyl)cinnoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
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