部分構造検索

C=CCCC.CCCCC

CCCCC[C@@H]1OC(=O)[C@@H]1CCCC
Reaction #41999
3-butyl-4-pentyl-oxetan-2-one
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CO[Si](C)(C)C(C)(C)C)[C@@H]1[C@@H]([C@@H](C)OC(=O)OCc2ccccc2)C(=O)N1C(Cc1ccc(OC)cc1)Cc1ccc(OC)cc1
Reaction #49995
(3S,4S)-4-(1-t-butyldimethylsilyloxymethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(Cc2ccc(OC)cc2)N2C(=O)[C@H]([C@@H](C)OC(=O)OCc3ccccc3)[C@@H]2C(C)CO[Si](C)(C)C(C)(C)C)cc1
Reaction #49996
(3S,4S)-4-(1-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di-(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66028
sucrose
収率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66029
sucrose
収率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@](CO)(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O
Reaction #66030
sucrose
収率 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCC1=CCCC1=O
Reaction #95250
2-(5-carbethoxypentyl)-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCOS(C)(=O)=O)c(OC)n2)c(OC)c1
Reaction #157846
4-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)butyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCN(C)C)c(OC)n2)c(OC)c1
Reaction #157847
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-[4-(dimethylamino)butyl]-6-methoxypyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)OCc8ccccc8)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172892
desired product
収率 14.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172893
desired product
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC1CCCN1C(=O)C(Cc1ccccc1)N(C)C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C
Reaction #173998
DOI: 10.1039/C8SC04228D
CC1(CC(O)CO)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C2C=CCC2)C1=O
Reaction #197711
DOI: 10.1039/C8SC04228D
CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)c4ccccc4)c4ccccc4)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O
Reaction #218931
paclitaxel
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(C2=CCCCC2)cc1N(C(=O)C1CCC(C)CC1)C1CCC(OC)CC1
Reaction #228662
DOI: 10.1039/C8SC04228D
CCCC1=[C]([TaH3][C]2=C(CCC)C=CC2)CC=C1
Reaction #236377
DOI: 10.1039/C8SC04228D
C=CC(CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)NCCOc1ccc(-c2ccccc2)cc1)C(C)C
Reaction #246649
DOI: 10.1039/C8SC04228D
CN(C)CC1CCN(C(=O)C(Cc2ccccc2)N(C)C(=O)C(Cc2ccc3ccccc3c2)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C)CC1
Reaction #265591
DOI: 10.1039/C8SC04228D
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