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38059

CC(C)CC(NC(=O)c1cccnc1SSc1ncccc1C(=O)NC(CC(C)C)C(=O)O)C(=O)O
Reaction #3352
title compound
Выход 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](S)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #49178
Thiocholesterol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.CCNC(=N)CCCSSc1ccccn1
Reaction #53250
Cholesterol ethylamidinopropyl-pyridyldisulfide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=C(C)COP(=O)(O)O)C(=O)OC2
Reaction #61304
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(O)c1CC=C(C)COP(=O)(O)O)C(=O)OC2
Reaction #61968
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC1CSC(=O)CN(C2CCCC2)C1=O
Reaction #63633
4-Cyclopentyl-6,7-dihydro-6-methyl-1,4-thiazepin-2,5-(3H,4H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc([N+](=O)[O-])cc2C(C(N)=O)=C1CC(F)(F)F
Reaction #64353
(2',2',2'-trifluoroethyl)-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCC1CC2C(CC(OC3CCCCO3)C2C=CC(CCCCC)OC2CCCCO2)S1
Reaction #252670
DOI: 10.1039/C8SC04228D
C#CC1C(C(C)O)C(=O)N1Cc1ccccc1
Reaction #334884
1-benzyl-4-ethynyl-3-(1-hydroxyethyl)-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=C(C)COP(=O)(O)O)C(=O)OC2
Reaction #359297
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(OCC[Si](C)(C)C)c1CC=C(C)COP(=O)(O)O)C(=O)OC2
Reaction #359402
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CCSSc1ccccn1)S(=O)(=O)O
Reaction #376239
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccccc2)nc(SSc2nc(-c3ccccc3)cc(C)c2C#N)c1C#N
Reaction #523629
brownish crystals
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #525075
1,9-lactone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #529587
1,9-lactone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC/C=C\C[C@@H]2[C@@H](CC[C@H](CCc3ccccc3)OC3CCCCO3)[C@H](OC3CCCCO3)C[C@@H]2O1
Reaction #604570
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC/C=C\C[C@@H]2[C@@H](/C=C/C(F)(F)COc3ccccc3)[C@H](OC3CCCCO3)C[C@@H]2O1
Reaction #604574
title compound
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(CC[C@@H]1[C@H]2C/C=C\CCCC(=O)O[C@H]2C[C@H]1OC1CCCCO1)O[Si](C)(C)C(C)(C)C
Reaction #604581
(8aR,9R,10R,11 aS,Z)-9-[3-(tert-butyldimethylsilyloxy)decyl)-10-(tetrahydro-2H-pyran-2-yloxy)-4,5,8,8a,9,10,11,11a-octahydrocyclo-penta[b]oxecin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c2c(c(O)c1CC=C(C)COP(=O)(O)O)C(=O)OC2
Reaction #627921
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CCSSc1ccccn1)S(=O)(=O)O
Reaction #680453
4-(pyridin-2-yldisulfanyl)-2-sulfobutanoic acid
Выход 30.2%DOI: 10.6084/m9.figshare.5104873.v1
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