بحث البنية الفرعية

512113

N#CC[C@@H]1C[C@H](CC(=O)O)OCO1
Reaction #5800
(±)-cis-6-(cyanomethyl)-1,3-dioxane-4-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
NCC[C@@H]1C[C@H](CC(=O)O)OCO1
Reaction #5801
(±)-cis-6-(2-aminoethyl)-1,3-dioxane-4-acetic acid
المردود 60.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)Nc2ccccc2)c(-c2ccccc2)c(-c2ccc(F)cc2)n1CC[C@H]1C[C@H](O)CC(=O)O1
Reaction #5802
trans-(±)-5-(4-fluorophenyl)-2-(1-methylethyl)-N,4-diphenyl-1-[2-(tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl]-1H-pyrrole-3-carboxamide
المردود 23.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](CCCCCC)C(=O)O1
Reaction #6156
(3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy]-6-undecyl-2H-pyran-2-one
المردود 63.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50189
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(O)C(F)(F)CCC[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC1CCCCO1
Reaction #50190
title compound ( 33 )
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
CCOC(=O)C(NCCCNC(=O)[C@@H](NC(=O)OCc1ccccc1)[C@H](C)O)[C@@H](O)[C@H]1O[C@H](n2ccc(=O)[nH]c2=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #54008
ethyl (5S)-12-[(R)-[(2R,3R,4R,5S)-3,4-bis(acetyloxy)-5-(2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl)tetrahydro-2-furanyl](hydroxy)methyl]-5-[(1S)-1-hydroxyethyl]-3,6-dioxo-1-phenyl-2-oxa-4,7,11-triazatridecan-13-oate
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NCCCNC(=O)[C@@H](NC(=O)OCc1ccccc1)[C@@H](O)C(C)C)[C@@H](O)[C@H]1O[C@@H](n2ccc(=O)[nH]c2=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #54010
ethyl (5S)-12-[(R)-[(2R,3R,4R,5R)-3,4-bis(acetyloxy)-5-(2,4-dioxo-3,4-dihydro-1(2H)-pyrimidinyl)tetrahydro-2-furanyl](hydroxy)methyl]-5-[(1S)-1-hydroxy-2-methylpropyl]-3,6-dioxo-1-phenyl-2-oxa-4,7,11-triazatridecan-13-oate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/[C@@H]1[C@H]2CC(=O)O[C@H]2C[C@H]1OC(=O)c1ccccc1)CCc1ccccc1
Reaction #96016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](c2ccc(Cl)c(Cc3ccc4c(c3)NCCO4)c2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #159758
(2S,3R,4R,5S,6R)-2-[4-chloro-3-(3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-phenyl]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCOc2ccc(Cc3cc([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)ccc3Cl)cc21
Reaction #159759
(2S,3R,4R,5S,6R)-2-[4-chloro-3-(4-ethyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-phenyl]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol
المردود 19.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O[C@H]1CCO[C@@H](C(c2ccccc2)c2ccccc2)C1
Reaction #166071
compound 4b
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@@H]1CCO[C@@H](C(c2ccccc2)c2ccccc2)C1
Reaction #166072
compound 5b
المردود 80.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCCC(C)(O)CO)C1CCC2C3C(Br)C=C4CC(O)CC(O)C4(C)C3CCC12C
Reaction #186987
DOI: 10.1039/C8SC04228D
CCN1CCOc2ccc(Cc3cc(C4OC(CO)C(O)C(O)C4O)ccc3Cl)cc21
Reaction #207671
DOI: 10.1039/C8SC04228D
CCCCCC(C=CC1C(OC2CCCCO2)CC2OC(C(Br)CCCC(=O)OC)CC21)OC1CCCCO1
Reaction #213779
DOI: 10.1039/C8SC04228D
CC(C)(Oc1ccc(Cl)cc1)C1CC(O)CC(=O)O1
Reaction #214479
desired Compound
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(O)CC(OC)(C2CSC(=O)N2Cc2ccc(OC)cc2)O1
Reaction #224053
DOI: 10.1039/C8SC04228D
الصفحة 1التالي