Impliqué dans 50 réactions

7415

CC(C)NCCS(=O)c1ccc(Cl)cc1
Reaction #4284
solid
Rendement 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O[B-]1(O)OO[B-](O)(O)OO1
Reaction #93840
perborate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(CCCCCO)c1ccc(-c2ccc(Cl)cc2Cl)cc1
Reaction #315074
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(O)/C=C\C(=O)O.O=S(=O)(c1ccc(Cl)cc1)C1CCN(Cc2ccccc2)C1
Reaction #323263
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
Cl.O=S(c1ccc(Cl)cc1)C1CCNCC1
Reaction #323278
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COCC(CO)COC
Reaction #339230
3-methoxy-2-methoxymethypropan-1-ol
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)OC(=O)N(Cc1cc(CCO)cc(Cl)c1Cl)C1CC1
Reaction #424734
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)[Si](C)(C)OCc1cc(CCO)cc(Cl)c1Cl
Reaction #424768
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COC(=O)c1cc(CCO)cc2ccccc12
Reaction #424781
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1cc(C(=O)O)c(Cl)cc1[N+](=O)[O-]
Reaction #443224
title product
Rendement 77.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
N#Cc1cc(F)c(N)c(I)c1
Reaction #487780
title product
Rendement 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COc1ccc2[nH]c(S(=O)Cc3ncc(C)c(OC)c3C)nc2c1
Reaction #515821
title compound
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
COc1ccc(N(CCCCO)S(=O)(=O)c2c(F)c(F)c(F)c(F)c2F)cc1
Reaction #516458
product
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
COC(=O)C1=CCCSC1
Reaction #526772
methyl 5,6-dihydro-2H-thiopyran-3-carboxylate
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
Cn1cc(-c2ccc(=O)n(Cc3cccc(-c4ncc(O)cn4)c3)n2)cn1
Reaction #561391
2-[3-(5-hydroxypyrimidin-2-yl)benzyl]-6-(1-methyl-1H-pyrazol-4-yl)-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)OC(=O)N1CCc2cc(O)cc(F)c2C1=O
Reaction #607497
tert-butyl 8-fluoro-6-hydroxy-1-oxo-3,4-dihydroisoquinoline-2(1H)-carboxylate
Rendement 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1ccc(N(CCCCO)S(=O)(=O)c2c(F)c(F)c(F)c(F)c2F)cc1
Reaction #809574
product
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
Cc1cc(-c2ccc3cc(O)ccc3c2Oc2ccc(OCCN3CCCCC3)cc2)ccc1S(C)(=O)=O.Cl
Reaction #819960
title compound
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CC(C)NCCS(=O)c1ccc(Cl)cc1
Reaction #832337
solid
Rendement 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
Cc1cc(-c2ccc3cc(O)ccc3c2Oc2ccc(OCCN3CCCCC3)cc2)ccc1S(C)(=O)=O.Cl
Reaction #836095
title compound
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
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