子结构搜索

551267

C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CO)C(=O)O
Reaction #64855
crude product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64856
product
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #87087
(2S,3R)-benzyl 2-((S)-2-((tert-butoxycarbonyl)amino)-3-hydroxypropanamido)-3-hydroxy-3-(4-methoxyphenyl)propanoate
收率 93.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@@H](N)CO)C(=O)OCc2ccccc2)cc1
Reaction #87088
(2S,3R)-benzyl 2-((S)-2-amino-3-hydroxypropanamido)-3-hydroxy-3-(4-methoxyphenyl)propanoate
收率 92.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COC(F)F)C(=O)N[C@@H](COC(F)F)C(=O)OCc1ccccc1
Reaction #89570
(S)-2-((S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionylamino)-3-di-fluoromethoxy-propionic acid benzyl ester
收率 65.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COC(F)F)C(=O)N[C@@H](COC(F)F)C(=O)O
Reaction #89571
(S)-2-((S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionylamino)-3-difluoromethoxy-propionic acid
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](NC(=O)[C@H](COC(F)F)NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89573
(S)-2-((S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionylamino)-3-methoxy-propionic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C(NC(=O)C(C)NC(=O)OC(C)(C)C)C(=O)O
Reaction #188408
DOI: 10.1039/C8SC04228D
CC(O)C(NC(=O)C(Cc1ccc(O)cc1)NC(=O)OC(C)(C)C)C(=O)O
Reaction #213052
DOI: 10.1039/C8SC04228D
CN1CC(c2ccc(F)cc2)C2(CCCN(C(=O)C(COCc3ccccc3)NC(=O)C(C)(C)NC(=O)OC(C)(C)C)C2)C1=O
Reaction #213709
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NN
Reaction #215020
tert-butyloxycarbonyl-L-phenylalanyl-L-serine hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CC1NC(=O)C(COCc2ccccc2)N(Cc2ccc(F)cc2)C1=O
Reaction #227947
DOI: 10.1039/C8SC04228D
O=C1C(CO)N(Cc2ccccc2)C(=O)C2COCCN12
Reaction #231734
DOI: 10.1039/C8SC04228D
CC(OCc1ccccc1)C(NC(=O)C(C)(C)NC(=O)OC(C)(C)C)C(=O)O
Reaction #253925
DOI: 10.1039/C8SC04228D
COC(=O)C(CO)NC(=O)[C@@H](C)NC(=O)OC(C)(C)C
Reaction #333118
2-((R)-2-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester
收率 45.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1COC([C@@H](C)NC(=O)OC(C)(C)C)=N1
Reaction #333119
2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
收率 95.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](CO)C(=O)N2CCSCC12
Reaction #508419
title compound
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)O
Reaction #514540
title compound
收率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](COCc1ccccc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #522585
[ 28 ]
收率 875.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](COCc1ccccc1)C(=O)NN
Reaction #522586
[ 29 ]
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
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