子结构搜索

CCCCO

CC(S)S(=O)(=O)O.N=C(N)NCCC[C@H](N)C(=O)O
Reaction #5585
white crystalline product
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(O[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6131
expected product
收率 81.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1O[C@@H]1SC[C@@H](O)[C@H](O)[C@H]1O
Reaction #6143
expected product
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1OC1C(=O)[O-].[K+].[K+]
Reaction #8648
potassium epoxysuccinate
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCC[C@H](N)C(=O)O
Reaction #8950
L-arginine
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCC[C@H](N)C(=O)O
Reaction #8953
L-arginine
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCC[C@H](N)C(=O)O
Reaction #8957
L-arginine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CCC(=O)O
Reaction #43561
4,4-dimethyl-pentanoic acid
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)COC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #51324
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C(O)C(=O)O
Reaction #54862
racemic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNN=C(C(=O)OCC)C(C)C
Reaction #59249
crude product ( 3b )
收率 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(OC2CN(c3ccc([C@H](C)NC(=O)C4(C)CCC4)cc3)C2)cc1
Reaction #68790
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNCCc1ccc(CC(C)(C)C(=O)O)cc1
Reaction #76091
3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1O[C@H]1C(=O)O
Reaction #82144
Cis-Epoxysuccinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)[C@@H]1CC[C@H](O)C1)C(=O)O
Reaction #87154
(R)-2-((1R,3S)-3-hydroxycyclopentanecarboxamido)propanoic acid
收率 131.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C[C@H]1CCc2c1[nH]c1ccc(OCc3ccc(C4CCCC4)c(C(F)(F)F)c3)cc21
Reaction #91085
(R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetate
收率 44.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(C(=O)Cl)c1ccc(Cl)cc1
Reaction #95323
2-isopropyl-2-p-chlorophenyl acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCCNC1
Reaction #157088
3-methylpiperidine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157089
3-methyl-(3-nitropyridin-4-yl)piperidine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
第 1 页下一页