Substructure Search

12632

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Reaction #6879
material
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #6880
material
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c[nH]c2c(F)cc(F)cc12)N(Cc1ccccc1)Cc1ccccc1
Reaction #8211
dibenzyl-[2-(5,7-difluoro-1H-indol-3-yl)-1(S)-methyl-ethyl]-amine
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc(C=O)cc1
Reaction #9072
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cccs2)cc1
Reaction #9074
title compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3F)oc2c1
Reaction #9702
(1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Yield 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #9710
desired compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C#Cc2ccccc2)cc1
Reaction #40793
1-(2-p-Tolylethynyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCC1CCCO1
Reaction #47111
product 477
Yield 60.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3F)oc2c1
Reaction #59201
(1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Yield 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #59209
desired compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74724
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(C3)C2C(=O)N1O
Reaction #74879
N-hydroxy-5-norbornene-2,3-dicarboximide
DOI: 10.6084/m9.figshare.5104873.v1
CONC(=O)c1ccccc1Nc1cc(Nc2cnn(C)c2C)ncc1Cl
Reaction #90781
desired product
Yield 7.3%DOI: 10.6084/m9.figshare.5104873.v1
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #90782
desired product
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2ccoc2)c1OCC(=O)NN
Reaction #91647
2-(2-(furan-3-yl)-6-methylphenoxy)acetohydrazide
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)[O-].OC[C@H]1O[C@H](OC[C@H]2O[C@H](O[C@]3(CO)O[C@H](CO)[C@@H](O)[C@@H]3O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O
Reaction #93704
raffinose oleate
Yield 85.2%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@H](OC2[C@@H](O)[C@H](O)C(O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O
Reaction #161669
Galactinol
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)COCC1CCC(COCC2CO2)O1
Reaction #180192
DOI: 10.1039/C8SC04228D
O=C(O)COc1cc(CNc2nc3ccccc3n2C2OC(CO)C(O)C2O)ccc1-c1ccccc1
Reaction #185577
DOI: 10.1039/C8SC04228D
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