Substructure Search

CC(NCCN)O

CC(C)(C)OC(=O)C(O)N1C(=O)[C@@H](NC(=O)COc2ccccc2)[C@H]1SCC(=O)C1COC(=O)C1
Reaction #6389
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H]2COC(C)(C)N2C(=O)OC(C)(C)C)n1)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47474
(R)-4-(3-{(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoylamino}-pyrazol-1-ylmethyl)-2,2-dimethyl-oxazolidin-3-carboxylic acid t-butyl ester
Yield 105.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H](N)CO)n1)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47475
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid [1-((R)-2-amino-3-hydroxy-propyl)-1H-pyrazol-3-yl]-amide
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccc(C(=O)c2ccc(Cl)cc2)c1)OCCN1CCN(c2ccc(Cl)cc2)CC1
Reaction #54291
2-[4-(4-chlorophenyl)-1-piperazinyl]-ethyl 3-(4-chlorobenzoyl)-benzeneacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)NC1(OC)C(=O)N2C(C(=O)O)=C(C)CSC21)n1cccc1
Reaction #54602
7-[[2-Carboethoxy-2-(1-pyrryl)acetyl]amino]-7-methoxy-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N(C2CCCCO2)C1CCOC1CCCCO1
Reaction #56306
1-(2-tetrahydropyranyl)-3-phenylacetamido-4-[2-(2-tetrahydropyranyl)oxyethyl]-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63611
intermediate 121
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1NC(=O)CN1CCNC(CO)C1
Reaction #63613
N-(5-fluoro-2-methylphenyl)-3-(hydroxymethyl)-1-piperazineacetamide
Yield 59.4%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(C(OCCCN2CCN(c3ncccn3)CC2)c2ccccc2)cc1
Reaction #63647
title compound
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C(OCCCN2CCN(c3cncc(Cl)n3)CC2)c2ccc(F)cc2)cc1
Reaction #63648
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(=O)OC1c2ccccc2C(=O)N1CCN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83941
desired product
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCOC2(C(O)C(C)(O)CO)NC(=O)C1(O)NC2=O
Reaction #173813
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC(C(=O)CSC2C(NC(=O)Cc3ccccc3)C(=O)N2C(O)C(=O)OCc2ccc(OC)cc2)O1
Reaction #185896
DOI: 10.1039/C8SC04228D
CC(C)N(CC1COC(C)(C)N1C(=O)OC(C)(C)C)c1ccccc1
Reaction #187226
DOI: 10.1039/C8SC04228D
O=C1CN2CCOC2(c2ccccc2F)c2cc(Cl)ccc2N1CCO
Reaction #190098
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)Cn1c(-c2ccccc2)ccc(NC(=O)NCc2ccccc2)c1=O)(O[SiH](C)C)C(C(C)(C)C)C(F)(F)F
Reaction #211463
DOI: 10.1039/C8SC04228D
Nc1ccn(C2OC(CO)C(O)N(c3ncccn3)C2O)c(=O)n1
Reaction #222015
DOI: 10.1039/C8SC04228D
C#CCc1c(C)nc2c(OC(NC(=O)CN)c3ccccc3C)cccn12
Reaction #233630
DOI: 10.1039/C8SC04228D
CCOCc1nc2c(N)nc3ccccc3c2n1CCN1C(C)=NOC1(C)C
Reaction #239420
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(CNc2ccccc2)COC1(C)C
Reaction #254561
DOI: 10.1039/C8SC04228D
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