Участвует в 182 реакциях

COCOC

COCn1c(-c2ccccc2)nc(C(F)(F)F)cc1=O
Reaction #1551
3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)c1cccc(-c2ccc(COc3ccc(C(=O)O)c(O)c3)cc2)c1
Reaction #46715
4-(3′-Acetyl-biphenyl-4-ylmethoxy)-2-hydroxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCOc1ccc([N+](=O)[O-])c(F)c1
Reaction #49790
title product
Выход 31.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=[N+]([O-])c1ccc(O)c(CCl)c1
Reaction #52567
2-chloromethyl-4-nitrophenol
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCC#N
Reaction #54196
propionitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Cn1c(C(F)(F)F)cc(=O)n(-c2ccc3snc(C4OCCO4)c3c2)c1=O
Reaction #77283
title compound
Выход 17.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](OCOC)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95332
17β-acetoxy-3β-methoxymethoxy-1α-methyl-17α-n-propyl-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COC(=O)C1CC(C#N)(c2ccc(OC)c3oc4ccccc4c23)CCC1=O
Reaction #176690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1ccc(-c2ccc(CC(=O)NCc3cccc(F)c3)cn2)cc1
Reaction #185002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCOCC1Oc2c(OC)cccc2C1=O
Reaction #191898
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #193017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)Cc2ccccc2CN1
Reaction #234186
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1S(=O)(=O)N1Cc2ccccc2CC1(C)C
Reaction #302662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)OCc2cc([C@@H]3CN(CCCCCCOCCOCc4cccc(-c5cccc(O)c5)c4)C(=O)O3)ccc2O1
Reaction #306221
title compound
Выход 45.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COCOc1ccc(Br)cc1
Reaction #309254
desired product
Выход 57.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC1(NS(=O)C(C)(C)C)CCC(NC(=O)OC(C)(C)C)CC1
Reaction #333833
tert-butyl 4-(1,1-dimethylethylsulfinamido)-4-methylcyclohexylcarbamate
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COCOc1ccc(Br)cc1
Reaction #335745
4-Methoxymethoxy-1-bromobenzene
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
COCOc1ccc(F)cc1Br
Reaction #339412
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCC12CC[C@@](C(=O)O)(OCOC1)C2(CC)CC
Reaction #342337
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)c1ccc2c(c1)COCCC2
Reaction #347445
8-tert-butyl-1,3,4,5-tetrahydro-2-benzoxepine
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
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