S- and Se-Nucleophiles
        For reactivities of structurally related compounds go to: Nucleophiles    
        Found 33 Molecules.
    
| Molecule | Solvent | Reactivity Parameters | Classification | Reference (sort by title or year) | 
|---|---|---|---|---|
![]() dimethylsulfide (in CH2Cl2)  | dichloromethane | N  Parameter: 12.32 sN Parameter: 0.72  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() dimethylselenide (in CH2Cl2)  | dichloromethane | N  Parameter: 12.60 sN Parameter: 0.72  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() dibutylsulfide (in CH2Cl2)  | dichloromethane | N  Parameter: 11.86 sN Parameter: 0.74  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() tetrahydrothiophene (in CH2Cl2)  | dichloromethane | N  Parameter: 13.10 sN Parameter: 0.72  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() tetrahydrothiopyran (in CH2Cl2)  | dichloromethane | N  Parameter: 11.94 sN Parameter: 0.75  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() phenylsulfinate (in DMSO)  | DMSO | N  Parameter: 19.60 sN Parameter: 0.60  | J. Am. Chem. Soc. 2010, 132, 4796-4805 DOI: 10.1021/ja9102056  | |
![]() 4-nitrothiophenolate (in DMSO)  | DMSO | N  Parameter: 18.92 sN Parameter: 0.87  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 3,5-bis(trifluoromethyl)thiophenolate (in DMSO)  | DMSO | N  Parameter: 19.71 sN Parameter: 0.86  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 4-(trifluoromethyl)thiophenolate (in DMSO)  | DMSO | N  Parameter: 21.30 sN Parameter: 0.86  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 3-(trifluoromethyl)thiophenolate (in DMSO)  | DMSO | N  Parameter: 21.75 sN Parameter: 0.86  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 3-chlorothiophenolate (in DMSO)  | DMSO | N  Parameter: 22.50 sN Parameter: 0.78  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 4-bromothiophenolate (in DMSO)  | DMSO | N  Parameter: 22.80 sN Parameter: 0.78  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() thiophenolate (in DMSO)  | DMSO | N  Parameter: 23.36 sN Parameter: 0.74  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 4-methylthiophenolate (in DMSO)  | DMSO | N  Parameter: 24.35 sN Parameter: 0.69  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() naphthalene-2-thiolate (in DMSO)  | DMSO | N  Parameter: 22.55 sN Parameter: 0.83  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() 4-methoxythiophenolate (in DMSO)  | DMSO | N  Parameter: 24.97 sN Parameter: 0.68  | J. Org. Chem. 2021, 86, 5965-5972 DOI: 10.1021/acs.joc.1c00025  | |
![]() thiocyanate (in MeCN)  | MeCN | N  Parameter: 17.94 sN Parameter: 0.60  | J. Am. Chem. Soc. 2003, 125, 14126-14132 DOI: 10.1021/ja037317u  | |
![]() phenylsulfinate (in MeCN)  | MeCN | N  Parameter: 20.11 sN Parameter: 0.59  | J. Am. Chem. Soc. 2010, 132, 4796-4805 DOI: 10.1021/ja9102056  | |
![]() thioacetate (in MeCN)  | MeCN | N  Parameter: 21.20 sN Parameter: 0.63  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() O-ethyl dithiocarbonate (in MeCN)  | MeCN | N  Parameter: 19.30 sN Parameter: 0.69  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() O-isopropyl dithiocarbonate (in MeCN)  | MeCN | N  Parameter: 18.27 sN Parameter: 0.78  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() N,N-dimethyl dithiocarbamate (in MeCN)  | MeCN | N  Parameter: 20.93 sN Parameter: 0.69  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() pyrrolidin-1-yl dithiocarbamate (in MeCN)  | MeCN | N  Parameter: 22.40 sN Parameter: 0.63  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() piperidin-1-yl dithiocarbamate (in MeCN)  | MeCN | N  Parameter: 23.84 sN Parameter: 0.57  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() 4-methylpiperazin-1-yl dithiocarbamate (in MeCN)  | MeCN | N  Parameter: 23.61 sN Parameter: 0.57  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() morpholin-1-yl dithiocarbamate (in MeCN)  | MeCN | N  Parameter: 21.72 sN Parameter: 0.64  | Org. Biomol. Chem. 2011, 9, 8046-8050 DOI: 10.1039/c1ob06245j  | |
![]() dimethylsulfide (in MeCN)  | MeCN | N  Parameter: 12.70 sN Parameter: 0.72  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() tetrahydrothiophene (in MeCN)  | MeCN | N  Parameter: 13.30 sN Parameter: 0.72  | Chem. Eur. J. 2021, 21, 11367-11376 DOI: 10.1002/chem.202100977  | |
![]() SO3(2-) (in water)  | water | N  Parameter: 16.83 sN Parameter: 0.56  | J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y  | |
![]() 2-sulfidoacetate (in water)  | water | N  Parameter: 22.62 sN Parameter: 0.43  | J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y  | |
![]() cysteine (dianionic, in water)  | water | N  Parameter: 23.43 sN Parameter: 0.42  | Org. Biomol. Chem. 2007, 5, 3814-3820 DOI: 10.1039/b713778h  | |
![]() glutathione GSH(NH3+/S-)  | water | N  Parameter: 20.97 sN Parameter: 0.56  | Angew. Chem. Int. Ed.  2019, 58, 17704-17708 DOI: 10.1002/anie.201909803  | |
![]() phenylsulfinate (in 50W50AN)  | water-MeCN mix | N  Parameter: 13.75 sN Parameter: 0.68  | J. Am. Chem. Soc. 2010, 132, 4796-4805 DOI: 10.1021/ja9102056  | 
































