子结构搜索

5699

CC(C)(C)OC(=O)N[C@@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #1283
N-[(1,1-Dimethylethoxy)carbonyl]-O-(2-nitrophenyl)-L-serine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #1417
N-[(1,1-Dimethylethoxy)carbonyl]-O-(2-nitrophenyl)-L-serine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2018
N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)N[C@@H](COC)[C@@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1cccc(F)c1
Reaction #41409
N-[(1S)-(2S)-(3-fluorophenyl)-2-{[1-(4-fluorophenyl)-1H-indazole-5-yl]oxy}-1-(methoxymethyl)ethyl]-2-methoxyacetamide
收率 7.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCOC[C@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #46097
N-tert-butoxycarbonyl-O-(4-pentenyl)-L-serine
收率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OCc1ccccc1)[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)O
Reaction #54609
Boc-Thr(Bzl)-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OH
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OCc1ccccc1)[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O)[C@@H](C)OCc1ccccc1
Reaction #54612
Boc-Thr(Bzl)-Thr(Bzl)-Lys(Z)-OH
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #65318
N-Boc-O-benzylserine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](C=O)COCc1ccccc1
Reaction #65319
N-Boc-O-benzylserinal
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #81402
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](COc1ccccc1N)C(=O)O
Reaction #81403
product
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NC(=O)OC(C)(C)C)(C(=O)OCC)C(=O)OCC
Reaction #86024
title compound
收率 86.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OC(C)(C)C)(C(=O)O)C(=O)OCC
Reaction #86025
title compound
收率 108.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(=O)OCC
Reaction #86029
title compound
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@](CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(=O)O
Reaction #86030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@](CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(N)=O
Reaction #86031
title compound
收率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](NC(=O)OC(C)(C)C)C(=O)OC
Reaction #86651
(S)-3-Allyloxy-2-tert-butoxycarbonylamino-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](N)C(=O)OC.Cl
Reaction #86652
(S)-3-Allyloxy-2-amino-propionic acid methyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CI)NC(=O)OC(C)(C)C
Reaction #87114
(R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate
收率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)OC(C)(C)C)C(=O)O)cc1
Reaction #87143
(2S,3R)-2-(tert-butoxycarbonylamino)-3-hydroxy-3-(4-methoxyphenyl)propanoic acid
收率 65.1%DOI: 10.6084/m9.figshare.5104873.v1
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