Substructure Search

C1COCN1

N#Cc1ccc(-c2csc(N3CCOC3=O)n2)cc1
Reaction #173
Yield 0.0%
CC[C@H]1CN(c2nc(/N=C/N(C)C)nc(C)c2Cc2ccc(CC#N)cc2)C(=O)O1
Reaction #184
Yield 45.7%
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CC3OC(=O)NC3=O)oc2c1
Reaction #1146
5-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-oxazolidinedione
Yield 6.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OCC1CNC(=O)O1
Reaction #3168
5-Acryloyloxymethyl-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)Oc2ccccc2O1
Reaction #5674
1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(N2CCOC2=O)c1
Reaction #44054
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCN1c1cccc(CCO)c1
Reaction #44131
title compound
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1c(C(=O)Nc2ccc(N3CCOC3=O)cc2)nc2ccccc21)Nc1ccc(Cl)cn1
Reaction #46814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49216
title compound
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49217
title compound
Yield 95.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)N2C(=O)OC[C@H]2Cc2ccccc2)NC1=O
Reaction #50253
N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-(R)-4-benzyl-2-oxazolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H](C)CCC(=O)N1C(=O)O[C@@H](c2ccccc2)[C@H]1C
Reaction #56711
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc(/C=C/C(=O)Nc2ccc(CC3OC(=O)NC3=O)cc2)c1-c1ccc(F)cc1
Reaction #58990
(2E)-N-{4-[(2,4-dioxo-1,3-oxazolidin-5-yl)methyl]phenyl}-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylamide
Yield 77.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CC(=O)N1C(=O)OC[C@@H]1c1ccccc1)c1ccccc1
Reaction #61114
(S)-4-phenyl-3-((S)-3-phenyl-butyryl)-oxazolidin-2-one
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCN1Cc1ccc([N+](=O)[O-])cc1
Reaction #72549
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCN1Cc1ccc([N+](=O)[O-])cc1F
Reaction #72581
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3N3CCOC3=O)nc2N1C1CCCC1
Reaction #73124
title compound
Yield 6.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H]1COC(=O)N1)(c1ccccc1)c1ccccc1
Reaction #85636
(R)-4-(((tert-butyldiphenylsilyl)oxy)methyl)oxazolidin-2-one
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(Cn2c3ccc(Br)cc3c3cc(Br)ccc32)O1
Reaction #90438
white solid
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(Cn2c3ccc(Br)cc3c3cc(Br)ccc32)CN1c1ccccn1
Reaction #90439
white solid
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1
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