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1180932

C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #46072
ethyl 1(R)-[1-tert-butoxycarbonyl-4(R)-hydroxypyrrolidine-2(S)-carboxamido]-2(S)-vinylcyclopropanecarboxylate
수율 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@H](O)CN1)C(=O)OCC.Cl
Reaction #46073
ethyl 1(R)-[4(R)-hydroxypyrrolidine-2(S)-carboxamido]-2(S)-vinylcyclopropanecarboxylate hydrochloride
수율 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1C(=O)N2
Reaction #46089
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid ethyl ester
수율 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(O[Si](C)(C)C(C)(C)C)CN2C1=O
Reaction #46090
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
수율 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccccn3)CN2C1=O
Reaction #46099
14-tert-butoxycarbonylamino-2,15-dioxo-18-(pyridin-2-yloxy)-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
수율 57.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(Oc3ccc([N+](=O)[O-])cc3)CN2C1=O
Reaction #46100
14-tert-butoxycarbonylamino-18-(4-nitrophenoxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
수율 44.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(N)C(=O)OC.Cl
Reaction #61359
compound 20b
수율 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1(C(=O)O)CC1
Reaction #62373
title compound
수율 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)C1OC(=O)C1(NC(=O)OCc2ccccc2)CC1
Reaction #63716
N-Cbz-1-aminocyclopropanecarboxylic acid 2,2,5,5-tetramethylcyclopentyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)C1OC(=O)C1(N)CC1
Reaction #63717
1-aminocyclopropylcarboxylic acid 2,2,5,5-tetramethylcyclopentyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NC3(C(=O)O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172738
title compound
수율 25.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CC1(NC(=O)C1CC2CC1C(=O)O2)C(=O)OCC
Reaction #180836
DOI: 10.1039/C8SC04228D
C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(OC(=O)N2Cc3cccc(F)c3C2)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #192767
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CC(OC(=O)c2ccc([N+](=O)[O-])cc2)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #198312
DOI: 10.1039/C8SC04228D
Cl
Reaction #202156
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CN(C(=O)OC(C)(C)C)Cc2c[nH]nc21)C(=O)NS(=O)(=O)C1CC1
Reaction #209901
DOI: 10.1039/C8SC04228D
CC1(C)CCC(C)(C)C1OC(=O)C1(N)CC1
Reaction #210424
DOI: 10.1039/C8SC04228D
C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(OC(=O)N2Cc3cccc(F)c3C2)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #211552
DOI: 10.1039/C8SC04228D
CC(NC(=O)C1(NC(=O)C(F)(F)F)CC1)c1ccc(Br)cc1F
Reaction #223603
DOI: 10.1039/C8SC04228D
C#Cc1cnn(-c2ccc(S(=O)(=O)NC3(C(=O)O)C(C)C3c3ccccc3)s2)c1
Reaction #231729
DOI: 10.1039/C8SC04228D
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