部分構造検索

512895

CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #49221
title compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #49222
title compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1
Reaction #49226
2-(tributylstannyl)oxazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1C[C@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(O)cc(N3CCCC3=O)c2)N(C(=O)OC(C)(C)C)C1
Reaction #49228
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CCCCN1C(c1ccccc1)c1ccccc1
Reaction #220119
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #264719
DOI: 10.1039/C8SC04228D
C=CCO[C@@H]1C[C@H](C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #689530
1-tert-butyl 2-methyl (2R,4R)-4-allyloxypyrrolidine-1,2-dicarboxylate
収率 96.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](OCC(O)CO)CN1C(=O)OC(C)(C)C
Reaction #689531
1-tert-butyl 2-methyl (2R,4R)-4-(2,3-dihydroxypropoxy)pyrrolidine-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1
Reaction #949419
title product
収率 46.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #1102048
title compound
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #1102049
title compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1
Reaction #1102053
2-(tributylstannyl)oxazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1C[C@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(O)cc(N3CCCC3=O)c2)N(C(=O)OC(C)(C)C)C1
Reaction #1102055
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H]1C[C@H](C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #1178457
1-tert-butyl 2-methyl (2R,4R)-4-allyloxypyrrolidine-1,2-dicarboxylate
収率 96.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](OCC(O)CO)CN1C(=O)OC(C)(C)C
Reaction #1178458
1-tert-butyl 2-methyl (2R,4R)-4-(2,3-dihydroxypropoxy)pyrrolidine-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(OCC(O)CO)CN1C(=O)OC(C)(C)C
Reaction #1204105
DOI: 10.1039/C8SC04228D
C=CCO[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1
Reaction #1544640
title product
収率 46.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C(=O)O)N(C(=O)OC(C)(C)C)C1
Reaction #1653957
DOI: 10.1039/C8SC04228D
C=CCO[C@@H]1C[C@@H](C(=O)OCC)N(C(=O)OC(C)(C)C)C1
Reaction #2272698
title compound
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1
Reaction #2317124
title product
収率 46.1%DOI: 10.6084/m9.figshare.5104873.v1