子结构搜索

15073

O=C(NCC(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #1844
Fmoc-Gly-Pro-Hyp
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H](O)C[C@H]1C(=O)O
Reaction #10036
title compound
收率 92.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](O)CN1C.Cl
Reaction #10037
title compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](OS(C)(=O)=O)CN1C
Reaction #10038
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@H](O)C[C@H]1C(=O)OC
Reaction #46087
1-(2(S)-tert-Butoxycarbonylamino-non-8-enoyl)-4(R)-hydroxy-pyrrolidine-2(S)-carboxylic acid methyl ester
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC1C=C(C(=O)O)N(C(=O)C(C)S)C1
Reaction #55888
(±)-4,5-dihydro-4-ethoxy-(2-mercapto-1-oxopropyl)-1H-pyrrole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](O[Si](C)(C)C(C)(C)C)CN1C
Reaction #62374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1[C@@H]2C[C@H](O)CN2C(=O)N1c1cc(Cl)cc(Cl)c1
Reaction #78243
titled compound
收率 23.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](Oc2ccc(Br)cc2)CN1
Reaction #78245
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](OCc2ccc(Br)cc2)CN1
Reaction #78247
above-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1[C@@H]2C[C@H](Oc3ccc(Br)cc3)CN2C(=O)N1c1cc(Cl)cc(Cl)c1
Reaction #78260
(7aS,6S)-2-(3,5-dichloro-phenyl)-6-(4-bromophenoxy)-tetrahydro-pyrrolo[1,2-c]imidazole-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1C[C@@H](O)CN1C(=O)OCc1ccccc1
Reaction #78414
desired product
收率 101.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](n2ccc(NC(=O)c3ccccc3)nc2=O)C[C@@H]1C(=O)OC(c1ccccc1)c1ccccc1
Reaction #79472
N-tert-butoxycarbonyl-cis-4-(N4-benzoylcytosin-1-yl)-D-proline diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC(O)CN1C(=O)OCC1c2ccccc2-c2ccccc21
Reaction #157934
Fmoc-Pro(4-OH)—OMe
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)N1CC2(C[C@H]1C(=O)OCc1ccccc1)OCCO2)C(C)C
Reaction #159145
(S)-benzyl 7-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-1,4-dioxa-7-azaspiro[4.4]nonane-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)N1CC2(C[C@H]1C(=O)O)OCCO2)C(C)C
Reaction #159146
desired product
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Oc2nc3cc(OC)ccc3nc2Cl)CN1C(=O)OC(C)(C)C
Reaction #159293
title compound
收率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)N1CC2(C[C@H]1C(=O)OCc1ccccc1)OCCO2)C(C)C
Reaction #167090
(S)-benzyl 7-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-1,4-dioxa-7-azaspiro[4.4]nonane-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)N1CC2(C[C@H]1C(=O)O)OCCO2)C(C)C
Reaction #167091
desired product
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](O)CN1
Reaction #168306
methyl (4R)-4-hydroxy-L-prolinate
DOI: 10.6084/m9.figshare.5104873.v1
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