methyl 5-(chloromethyl)-2-furoate

COC(=O)c1ccc(Cn2ncc([N+](=O)[O-])n2)o1
Reaction #71016
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #158529
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #163638
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(Cn2cc([N+](=O)[O-])cn2)o1
Reaction #175338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(CN2C(=O)C3(COc4cc5c(cc43)OCCO5)c3ccccc32)o1
Reaction #287493
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #313801
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1ccc(Cn2ccc([N+](=O)[O-])n2)o1
Reaction #397823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1ccc(Cc2c(C)cc(C)cc2C)o1
Reaction #408357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1ccc(COCC(F)(F)F)o1
Reaction #428748
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COC(=O)c1ccc(C)o1
Reaction #463778
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #492526
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COC(=O)c1ccc(CN2C(=O)N(c3cccc(C(F)(F)F)c3)C(C)=C(C(=O)C3CC3)C2c2ccc(C#N)cc2)o1
Reaction #508982
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)c1ccc(COc2ccc(CC(C)=O)cc2)o1
Reaction #552644
methyl 5-[4-acetonyl- phenoxymethyl]furan-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
COC(=O)c1ccc(CN2C(=O)N(c3cccc(C(F)(F)F)c3)C3=C(C(=O)CCC3)C2c2ccc(C#N)cc2)o1
Reaction #604428
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #615310
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #621537
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COC(=O)c1ccc(Cn2c(=O)n(O)c(=O)c3sc4ccccc4c32)o1
Reaction #637910
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #665447
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COC(=O)c1cc(COc2ccc([N+](=O)[O-])cc2)co1
Reaction #690773
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COC(=O)c1ccc(C)o1
Reaction #699483
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
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