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1014581

COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1COC[C@H]1OC(=O)C(C)Cl
Reaction #3176
(±)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(OCCOCCOCCO)c1
Reaction #5144
2-(2-(2-(3-nitrophenoxy)ethoxy)ethoxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6089
expected product
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H](OC(=N)C(Cl)(Cl)Cl)SC[C@H]1OC(C)=O
Reaction #6127
expected product
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(C#N)cc1
Reaction #6128
expected product
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(C(C)=O)cc1
Reaction #6133
expected product
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CNCCOCCOCCNCc2ccccc2)cc1
Reaction #6312
1,10-dibenzyl-4,7-dioxa-1,10-diazadecane
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1cccc(OC)c1
Reaction #41357
N-[(1R,2S)-1-[1-(4-Fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]-2-(2-methoxyethoxy)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1O[C@@H]1O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #48959
(2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(OC1C(Cl)=C(OC2=C(Cl)C(OC(C)C(=O)O)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-])C(=O)O
Reaction #55593
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-carboxyethoxy)-4-nitrophenyl ether
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)OC1C(Cl)=C(OC2=C(Cl)C(OC(C)CO)C(c3ccccc3C(F)(F)F)([N+](=O)[O-])C=C2)C=CC1(c1ccccc1C(F)(F)F)[N+](=O)[O-]
Reaction #55607
2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
OCCOCCOCCN1CCCC1
Reaction #62993
N-(hydroxyethoxyethoxyethyl)pyrrolidine
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@H](OCC(Cl)(Cl)Cl)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #68717
1-O-trichloroethyl-2,3,4-tri-O-acetyl-α-D-glucopyranuronic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCC(=O)Cl
Reaction #80940
3,6,9-trioxadecanoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #82192
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82906
Formula IX
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87478
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87498
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCC(=O)O[C@H]1[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #90566
212
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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