部分構造検索

1329141

COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)cccc1CO[C@H]1CCC[C@@H](O)C1
Reaction #10468
desired compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)cccc1CO[C@@H]1CCC[C@H](O)C1
Reaction #10469
methyl (1R,3S)-2-(3-hydroxycyclohexyloxymethyl)-6-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)cccc1CO[C@H]1CCC[C@@H](O)C1
Reaction #10477
desired compound
収率 14.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)cccc1CO[C@H]1CCC[C@@H](O)C1
Reaction #10478
desired compound
収率 14.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)cccc1CO[C@H]1CCC[C@@H](O)C1
Reaction #10479
desired compound
収率 13.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COC(=O)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O[Si](C)(C)C(C)(C)C)C(=O)N2CC(=O)OCc2ccc([N+](=O)[O-])cc2)cc1
Reaction #49987
(3S,4S)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-[(1R)-1-p-methoxybenzyloxycarbonylethyl]-1-(p-nitrobenzyloxycarbonylmethyl)azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #59438
MeOSuc-βAla-Leu-Ala-Leu-Dox
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74471
title compound
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)s1
Reaction #74474
title compound
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)s1
Reaction #74475
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc(C3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74485
3-(2-Chloro-5-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-6-ethoxypyridazine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cnc(Cc2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74492
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](CCC(=O)OCc1ccccc1)COS(C)(=O)=O
Reaction #78200
benzyl (4R)-4-t-butoxycarbonylamino-5-methanesulfonyloxypentanoate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1O[C@H](CO)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #82116
Allyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H]1O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1O
Reaction #92526
allyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCOc1cccc(OCCCCCOCc2ccccc2)c1
Reaction #161576
2-(2-(3-(5-benzyloxypentoxy)phenoxy)ethyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(OCCCCCOCc2ccccc2)c1
Reaction #161603
3-(5-(benzyloxy)pentyloxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #172891
desired product
収率 65.0%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
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