部分構造検索

CCCCCCC.C1CCOC1

Cc1[nH]c2ccccc2c1CN(C)C(=O)/C=C/c1cnc2c(c1)CCCC(=O)N2
Reaction #46612
title compound
収率 76.9%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
COc1ccc(Cn2c(=O)ccn([C@@H]3OC([C@H](O)[C@H](NC(=O)CCCCCCCCCCN)C(=O)OC(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)c2=O)cc1
Reaction #54005
tert-butyl (2S,3R)-2-[(11-aminoundecanoyl)amino]-3-[(3R,4R,5R)-3,4-bis{[tert-butyl (dimethyl)silyl]oxy}-5-(3-(4-methoxybenzyl)-2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl)tetrahydro-2-furanyl]-3-hydroxypropanoate
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)O[C@H]1CO[C@H]2[C@@H]1OC[C@H]2OC(=O)CCCCCCC
Reaction #90211
Isosorbide Dicaprylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC(O)C1CCC(CCC2CCCCC2)O1)C(F)(F)F
Reaction #91591
N-(3-(5-(2-cyclohexylethyl)tetrahydrofuran-2-yl)-3-hydroxypropyl)-2,2,2-trifluoroacetamide
DOI: 10.6084/m9.figshare.5104873.v1
NCCC(O)C1CCC(CCC2CCCCC2)O1
Reaction #91592
3-amino-1-(5-(2-cyclohexylethyl)tetrahydrofuran-2-yl)propan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(/C=C/CC(C)CCCC(C)(C)OC)=C1COC(=O)C1
Reaction #95403
aimed compound
収率 52.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(/C=C(/O)CC(C)CCCC(C)(C)OC)=C1COC(=O)C1
Reaction #95405
aimed compound
収率 63.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC1CC(C(=O)OCCOc2ccccc2)C(=O)O1
Reaction #187573
DOI: 10.1039/C8SC04228D
CC12CCC3C4=C(CCC3C1CCC21CC(O)CO1)CC(=O)CC4
Reaction #202965
DOI: 10.1039/C8SC04228D
CCCCCCCC(C=CC1C(O)CC2OC(O)CC21)OC1CCCCO1
Reaction #207394
DOI: 10.1039/C8SC04228D
CCCCCN(CCCNC(=O)C(NC(=O)C(NC(=O)NC(C(=O)O)C(C)C)C1CCNC(=N)N1)C(O)C(C)C)C(C(=O)O)C(OC1OC(CN)C(O)C1OC)C1OC(n2ccc(=O)[nH]c2=O)C(O)C1O
Reaction #207757
DOI: 10.1039/C8SC04228D
CC1(C)CCCC2(C)C1CCC1(C)OC(O)C(O)C12
Reaction #227460
DOI: 10.1039/C8SC04228D
CC1CC(C(CC2CCCCC2)NC(=O)C(Cc2cscn2)NC(=O)OC(C)(C)C)OC1=O
Reaction #232256
DOI: 10.1039/C8SC04228D
CCCCCC(O)C=CC1C(O)CC2OC(=CCCCC(=O)OCCN(CC)CC)CC21
Reaction #235004
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)C2CC(N(C(=O)C3CCCO3)C3CCC(C)(C)CC3)CN2C(=O)C2CN(C3CC3)CC2c2ccc(Cl)cc2)CC1
Reaction #235038
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCC1(COCc2ccccc2)COC(=O)C1
Reaction #236344
DOI: 10.1039/C8SC04228D
CCCCC(=O)Cc1ccn(C2OC(COC(=O)c3ccccc3)C(OC(=O)c3ccccc3)C2OC(=O)c2ccccc2)c(=O)n1
Reaction #240186
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N1CC2CCCCC(NC(=O)c3ccccc3)C(=O)N2C(C(=O)NC2CC(=O)OC2O)C1
Reaction #242721
DOI: 10.1039/C8SC04228D
CCC(O)(CC)C1CC(C(CC2CCCCC2)NC(=O)OC(C)(C)C)OC1=O
Reaction #247063
DOI: 10.1039/C8SC04228D
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