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CCOCC.FB(F)F

CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC1C=CC(=O)C1
Reaction #2643
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(C(c3c4c(c(C(=O)OC)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)OC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2695
Bis-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis (1,3) dioxol-4-yl)-mono-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methane
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](NC(=O)OCc1ccc(OC)cc1)C(=O)OCc1ccccc1
Reaction #3873
title compound
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
Reaction #5446
white solid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCCCCC1=O
Reaction #5485
2-ethoxycarbonyl-cyclononanone
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCCCCCC(C(=O)OCC)NC1=O
Reaction #5490
ethyl 3-methylidene-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cccc2cnccc12)N1Cc2cc(O)c(O)cc2CC1CN1CCN(c2ccccc2)CC1
Reaction #5816
title compound
Выход 90.9%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(CC2SCCCS2)cc1
Reaction #6482
title compound
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(S(=O)(=O)C[C@@H]2CC[C@H](OCc3ccccc3)C[C@H]2O)cc1
Reaction #7771
(±)(1R*,2R*,5S*)-5-benzyloxy-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexanol
Выход 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(S(=O)(=O)C[C@@H]2CCOC[C@H]2O)cc1
Reaction #7772
(±)(3S*,4R*)-4-(4-methylsulfanyl-benzenesulfonylmethyl)-tetrahydro-pyran-3-ol
Выход 35.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C2COC(=O)C2)cc1
Reaction #8296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(Cc2ccc(F)cc2)=NN2C(=O)CC[C@@H]2COCc2ccccc2)n1
Reaction #8326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cccc(F)c21
Reaction #9358
8-fluoro-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.c1ccc2c(c1)C1CNCC2C1
Reaction #10180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)O[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42654
(11β,16β)-21-(acetyloxy)-9-fluoro-11-hydroxy-16-methyl-3,20-dioxopregna-1,4-dien-17-yl ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCc2ccccc2)c2[nH]c(=O)ccc12
Reaction #42724
title compound
Выход 134.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc(Cl)cc1)c1ccc(O)cc1O
Reaction #42772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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