356 件の反応に参加

2017

O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #3086
3-[((4-chloroanilino) carbonyl)methyl]phenol
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #6538
3-[((4-chloroanilino) carbonyl)methyl]phenol
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCc1nn2c(-c3c(C)cc(C)cc3OC)ccc(OC)c2c1NC(CC)CC
Reaction #9301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(CC)Nc1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OC(C)(C)C)cc1)CC2
Reaction #11061
intermediate 11a
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(C#N)(CC)N1CCCC1
Reaction #49076
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(C#N)(CC)N(C)C
Reaction #49078
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=O)C(C)C(O)c1ccccc1
Reaction #50338
5-phenyl-5-hydroxy-4-methylpentan-3-one
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCC1(CC)OCC(CO)CO1
Reaction #59907
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC1(CC)OCC(COCc2ccccc2)O1
Reaction #59963
title compound
収率 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(CC)(c1ccc(O)cc1)c1ccc(O)cc1
Reaction #63710
3,3-Bis(p-hydroxyphenyl)pentane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCC(CC)N[C@H]1COc2c(F)ccc(OC)c2C1
Reaction #65949
(R)-8-fluoro-5-methoxy-3-(N-3-pentylamino)chroman
収率 176.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCC1(CC)OCCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Reaction #65983
pure title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCC(N)(CC)c1cccc(OCC2CC2)c1
Reaction #69065
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(O)(CC)CCCC(F)(F)F
Reaction #69620
7,7,7-trifluoro-3-ethyl-3-heptanol
収率 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cccc2nc(N3CC[C@@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@@H](NC(CC)CC)C3)sc12
Reaction #72129
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CCc1c(C(O)(CC)CC)ccnc1F
Reaction #75636
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=CCC(C)C(C)C1=O
Reaction #94079
2,5,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC1=CCC(C)C(C)C1=O
Reaction #94080
2,5,6-trimethyl-2-cyclohexen-1-one
収率 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC1=CCC(C)C(C)C1=O
Reaction #94081
2,5,6-trimethyl-2-cyclohexen-1-one
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC1=C(C)C(=O)C(C)CC1
Reaction #94083
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
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