Busqueda de Subestructura

347275

O=C(O)C1NCCC2CCCCC21
Reaction #1685
perhydro-1-isoquinolinecarboxylic acid
Rendimiento 56.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cc(F)ccc1SSc1ccc(F)cc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1cc(F)ccc1SSc1ccc(F)cc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3796
title compound
Rendimiento 17.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #4352
desired product
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #4355
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H]1C[C@H](O)[C@H](C2CCCCC2)NC1=O
Reaction #5653
(3S,5S,6S)-6-Cyclohexyl-5-hydroxy-3-isopropyl-piperidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](Br)CC1CCCCC1
Reaction #59363
(R)-α-bromocyclohexanepropionic acid
Rendimiento 27.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)NC(=O)OCc1ccccc1
Reaction #64787
N-[(Phenylmethoxy)carbonyl]-L-leucinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)NC(=O)OCc1ccccc1
Reaction #64807
N-[(Phenylmethoxy)carbonyl]-L-leucinamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(OCCCC)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)OCc1ccccc1
Reaction #65082
N-benzyloxycarbonyl-L-leucyl-L-argininal dibutyl acetal
Rendimiento 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC(CC1CCCCC1)NC(=O)OC(C)(C)C)CC(CC1CCCCC1)NC(=O)OC(C)(C)C
Reaction #67648
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)S[C@@H]1CC1CCCCC1
Reaction #74340
(5R)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)S[C@H]1CC1CCCCC1
Reaction #74342
(5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CC(C)C)NC(=O)C(Cc1ccc(OC)cc1)Sc1ccccc1Br
Reaction #78917
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1
Reaction #82333
L-proline tert.butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(C)cc1)[C@H](O)C(C)C
Reaction #91965
(2S,3R)-3-hydroxy-4-methyl-2-(toluene-4-sulfonylamino)-pentanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@@H](OS(C)(=O)=O)[C@H](NS(=O)(=O)NC(=O)OC(C)(C)C)C1
Reaction #92321
title compound
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@@H](OS(C)(=O)=O)[C@H](NS(=O)(=O)NC(=O)OC(C)(C)C)C1
Reaction #92322
title compound
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O[C@@H]2CC[C@H](C(=O)N(C)C)C[C@H]2NS(=O)(=O)NC(=O)OC(C)(C)C)cc1
Reaction #92324
title compound
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@@H]2NS(=O)(=O)N(C(=O)OC(C)(C)C)[C@@H]2C1
Reaction #92325
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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