Substructure Search

41778

CC1(C(F)(F)F)C[C@@H](O)c2cc(Br)ccc2O1
Reaction #48333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@H]1CCC(=O)N1CCSCCCC(=O)OC
Reaction #51247
4-[(2-{(2R)-2-[(1E,3S)-3-hydroxyoct-1-enyl]-5-oxopyrrolidin-1-yl}ethyl)thio]butanoic acid methyl ester
Yield 29.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@H]1CCC(=O)N1CCCCOCC(=O)OC
Reaction #51252
{4-[(R)-2-((E)-(S)-3-hydroxy-oct-1-enyl)-5-oxo-pyrrolidin-1-yl]-butoxy}-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CCN2C(=O)CC[C@@H]2/C=C/[C@H](O)CCC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1
Reaction #57059
Methyl 4-{2-[(2R)-2((1E,3R,7R)-7-{[tert-butyl(dimethyl)silyl]oxy}-3-hydroxyoct-1-enyl)-5-oxopyrrolidin-1-yl}ethyl}benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Oc1ccc2c(c1)CCCC2O)C(F)(F)F
Reaction #60381
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCC[C@H](O)c1ccc(F)cc1
Reaction #66006
methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate
Yield 98.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)c1c(C)nc2c(ccn2Cc2cccc(F)c2F)c1I
Reaction #201427
DOI: 10.1039/C8SC04228D
COCCCN1C[C@@H](O)c2cc(Cl)sc2S1(=O)=O
Reaction #217109
(S)-6-chloro-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazin-4-ol 1, 1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2CO2)cc1
Reaction #222049
DOI: 10.1039/C8SC04228D
O=S1(=O)CCC(O)c2ccsc21
Reaction #242543
DOI: 10.1039/C8SC04228D
O=C1C(CCC(O)c2ccc(F)cc2)C(c2ccc(OCc3ccccc3)cc2)N1c1ccc(F)cc1
Reaction #260705
DOI: 10.1039/C8SC04228D
O[C@H](CBr)c1ccc(Br)cc1
Reaction #305497
2-bromo-1-(1S)-(4-bromophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC[C@H](O)c1ccc2c(c1)COC(C)(C)O2
Reaction #306172
title compound
Yield 85.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]([C@@H](O)c2ccccc2)C1
Reaction #340726
(R)-tert-butyl 3-((R)-hydroxy(phenyl)methyl)piperidine-1-carboxylate
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]([C@@H](O)c2cccc(Cl)c2)C1
Reaction #340751
(R)-tert-butyl 3-((R)-(3-chlorophenyl)(hydroxy)methyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CC[C@@H](O)c1cccc(O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c1
Reaction #345663
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(C)c2c(c(O[Si](C)(C)C(C)(C)C)c1C[C@H](O)C1=CCCC1)C(=O)OC2
Reaction #347306
(S)-2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-1-cyclopentenyl-1-hydroxyethane
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCC(O)c1ccc(F)cc1
Reaction #370912
DOI: 10.1039/C8SC04228D
CC(C)(C)C1CCC(N(Cc2ccc(C(O)Cc3nn[nH]n3)cc2)C(=O)Nc2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #386251
DOI: 10.1039/C8SC04228D
O=c1ccc2c([C@@H](O)CBr)ccc(OCc3ccccc3)c2[nH]1
Reaction #419821
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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