#7977698

CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(/C=C/c2ccc3c(c2)C(SCC)=CCC3(C)C)cc1
Reaction #1467
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCN(CCC)C1CCc2cc(/C=C/C(=O)OC)ccc2C1
Reaction #1765
expected product
Yield 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc2c(c1)OC(c1ccc(OCCN3CCCCC3)cc1)c1c-2sc2ccccc12
Reaction #1804
title compound
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C=Cc1nc(CO)ccc1O
Reaction #1851
Ethyl 3-{3-hydroxy-6-hydroxymethylpyridin2-yl}propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5642
title compound
Yield 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)CC[C@H](NC(=O)c1ccc(C(=Cn2cnc3nc(NC(=O)C(C)(C)C)cc-3c2O)COC2CCCCO2)cc1)C(=O)OCC
Reaction #6625
diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC1CCN(CC#Cc2cccc(F)c2)CC1
Reaction #6886
oil
Yield 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(=O)[nH]c2ccccc12
Reaction #6907
methyl 2-oxo-1,2-dihydroquinoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(S(N)(=O)=O)s1
Reaction #7054
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(C)cc1Cl
Reaction #7065
methyl 2-chloro-4-methylbenzoate
Yield 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(CC(=O)Nc2cccc(/C=C/c3cccc(C)c3)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7178
4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide
Yield 152.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C1CCOc2cccnc21
Reaction #7224
title compound
Yield 52.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(-c2ccccc2-c2ccccc2)cc1
Reaction #7431
terphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(-c2nccc3ccccc23)cc1
Reaction #7432
1-phenylisoquinoline
Yield 96.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(-c2nc3ccccc3o2)ccc1-c1ccc(N2CCOCC2)cn1
Reaction #7887
2-[3-methoxy-4-(5-morpholin-4-ylpyridin-2-yl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
Reaction #8295
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C=Cc1ccc2c(-c3c(-c4cccc(C)n4)nn4c3CCC4)ccnc2c1
Reaction #8348
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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