Involved in 1654 reactions

1980

C#CCOc1cc(-n2nc(CCC=O)[nH]c2=O)c(Cl)cc1Cl
Reaction #2061
title product
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CCC(O)CO
Reaction #8282
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)CC(NC(=O)c1ccccc1)[Si](C)(CCC(=O)O)c1ccccc1
Reaction #8643
3-[[1-(Benzoylamino)-3-methylbutyl]methylphenylsilyl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=CCCCN1CCCCCCC1=O
Reaction #10276
4-(2-oxo-azocan-1-yl)-butyraldehyde
Yield 0.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CN2C(=O)c3c(-c4ccccc4Cl)cc4c(c3C2=O)c2cc(OC)ccc2n4CC(O)CO)c(OC)c1
Reaction #11227
diol
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cc2c(nn1)OCCC2
Reaction #43429
product
Yield 54.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCS2
Reaction #43431
solid
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)SCCO2
Reaction #43433
solid
Yield 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCO2
Reaction #43450
solid
Yield 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCC2
Reaction #43458
product
Yield 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCc2ccc(C=O)cc2C1=O
Reaction #43635
product
Yield 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C=O)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45739
compound
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c2c(c3n(c1=O)CC(CO)OC3=O)CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=CCCCc1nccc(-c2ccccc2)n1
Reaction #47941
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=CCCCc1nccc(C(F)(F)F)n1
Reaction #47943
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(OCc1ccccc1)N1CCC(n2c(=O)[nH]c3nnccc32)CC1
Reaction #48363
product
Yield 6.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](C)(C)OCCONC(=O)c1cc(CNC(=O)C=O)c(F)c(F)c1Nc1ccc(I)cc1F
Reaction #49054
N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-oxo-acetylamino)-methyl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](c1ccccc1)(c1ccccc1)C(O)[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)[C@H](OCCO)[C@@]1(O)[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #51524
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #53397
Compound 31
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC(O)CO)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57149
title compound
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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