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10958

CC(=O)C(C(C)=O)C(=O)C(C)Oc1ccc(Oc2ccc(Br)cc2F)cc1
Reaction #4560
product
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1
Reaction #5069
2-(Diphenylmethyl)-1-azabicyclo[2.2.2]octan-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
OC(CC1CN(CCc2ccc(F)cc2F)C1)c1ccccc1
Reaction #10314
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2CC3CCCCC3(O2)C1=C
Reaction #11001
product
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(/C=C/[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC1CCCCO1)O[Si](C)(C)C(C)(C)C
Reaction #50191
title compound ( 46 )
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccnc3c2ccn3COCC[Si](C)(C)C)cc1C1CCCC(O)C1
Reaction #69159
desired product
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccnc3c2ccn3COCC[Si](C)(C)C)cc1C1CCCC(O)C1
Reaction #73192
desired product
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C2Cc3c(ccc(F)c3F)C(C2)C1O
Reaction #77436
5.6-Difluoro-10,11-dihydroxytricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N[C@@H]1COC(C)(C)C[C@H]1O)c1ccccc1
Reaction #84711
(4R,5R)-2,2-dimethyl-5-((R)-1-phenylethylamino)-tetrahydro-2H-pyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C[C@H](O)[C@@H](N)CO1
Reaction #84717
title compound
収率 189.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CO[C@H]([C@H](CO)Cc1ccc(C)cc1)[C@H](C)OCc1ccccc1
Reaction #87228
(2S,3R,4S)-4-(benzyloxy)-3-((2-methylallyl)oxy)-2-(4-methylbenzyl)pentan-1-ol
収率 63.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CN(Cc2ccccc2)[C@@H]1C(=O)OCc1ccccc1
Reaction #89718
alcohol
収率 100.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CN[C@@H]1C(=O)O
Reaction #89719
(2S,3S,5R)-5-hydroxy-3-(methoxycarbonyl)piperidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@H](OC)CN(Cc2ccccc2)[C@@H]1C(=O)OCc1ccccc1
Reaction #89749
methyl ether
収率 3.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@H](OC)CN[C@@H]1C(=O)O
Reaction #89750
(2S,3S,5S)-5-methoxy-3-(methoxycarbonyl)piperidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](C2CC2)C[C@H]1CO)c1ccccc1
Reaction #155616
product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c([C@]23CO[C@@H](C4CC4)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)c1
Reaction #155617
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C2CC(OC(C)=O)CCC2NC(=O)c2ccc(OC)nc2OC)ccc1OC
Reaction #160673
crude title compound
収率 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc2c3c([nH]c12)C(CC)(CC(C)=O)OCC3
Reaction #190397
DOI: 10.1039/C8SC04228D
COC(=O)C1C(c2ccc(F)c(C)c2)=CC(O)CC1(C)C
Reaction #191253
DOI: 10.1039/C8SC04228D
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