Recherche de Sous-structure

O=C1CCCC(=O)O1

CC12CCC(C(=O)N(CCCCN3CCN(c4ncccn4)CC3)C1=O)C2(C)C
Reaction #5013
title compound
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCC(C2)C(=O)N1CCCCN1CCN(c2ncccn2)CC1
Reaction #5014
title compound
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCC(C2)C(=O)N1CCCCN1CCN(c2ncccn2)CC1
Reaction #5015
title compound
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2CCC1C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #5016
title compound
Rendement 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC(C)(C1)C(=O)N(CCCCN1CCN(c3ncccn3)CC1)C2=O
Reaction #5017
title compound
Rendement 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1C2
Reaction #5020
anhydride
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC(=O)O.O=C1CCC(=O)N1O
Reaction #6431
mono N-hydroxysuccinimide glutarate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCO)CCO
Reaction #7102
3,3-dimethyl-1,5-pentanediol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1)[C@H]1C[C@H]1C(=O)O
Reaction #9637
cis-2-(4-bromobenzoyl)cyclopropanecarboxylic acid
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)CCCC(=O)O)CC2)c1
Reaction #42606
5-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[1-(3-ethylphenyl)cyclopropyl]amino}-2-hydroxypropyl)amino]-5-oxopentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(NC(=O)CCCC(=O)O)c1
Reaction #47736
product
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(NC(=O)CCCC(=O)O)cc1
Reaction #47737
yellow white product 24
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC(=O)O.O=C1CCC(=O)N1
Reaction #53751
succinimide glutarate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(C2CC(=O)OC(=O)C2)cc1
Reaction #55647
3-(4-acetyloxyphenyl)glutaric anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(CCC2CC(=O)OC(=O)C2)cc1
Reaction #55651
3-[2-[4-(acetyloxy)phenyl]ethyl]glutaric anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(CCCC2CC(=O)OC(=O)C2)cc1
Reaction #55653
3-[3-[4-(acetyloxy)phenyl]propyl]glutaric anhydride
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c2[nH]cnc2n(C)c1=O
Reaction #56342
Theophylline
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1)[C@H]1C[C@H]1C(=O)O
Reaction #59134
cis-2-(4-bromobenzoyl)cyclopropanecarboxylic acid
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NN(Cc2ccccc2)C(=O)C2CC12
Reaction #65146
titled compound
Rendement 29.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1NC(=O)C2C(C1=O)C2(C)C
Reaction #65147
titled compound
Rendement 27.4%DOI: 10.6084/m9.figshare.5104873.v1
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