Search

Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
dimethoxymethane![]() ![]() |
dichloromethane | N Param.: -4.90 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-methyl-1,3-dioxolane![]() ![]() |
dichloromethane | N Param.: -3.30 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
4,5-dimethyl-1,3-dioxolane (anti)![]() ![]() |
dichloromethane | N Param.: -2.40 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2,4,5-trimethyl-1,3-dioxolane (anti)![]() ![]() |
dichloromethane | N Param.: -3.00 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-ethyl-4,5-dimethyl-1,3-dioxolane (anti)![]() ![]() |
dichloromethane | N Param.: -2.90 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
4,5-dimethyl-2-vinyl-1,3-dioxolane![]() ![]() |
dichloromethane | N Param.: -2.60 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-isopropyl-4,5-dimethyl-1,3-dioxolane (ani)![]() ![]() |
dichloromethane | N Param.: -4.10 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2,4,5-trimethyl-1,3-dioxolane (syn)![]() ![]() |
dichloromethane | N Param.: -2.50 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-ethyl-4,5-dimethyl-1,3-dioxolane (syn)![]() ![]() |
dichloromethane | N Param.: -2.40 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-isopropyl-4,5-dimethyl-1,3-dioxolane (syn)![]() ![]() |
dichloromethane | N Param.: -3.50 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
1,3-dioxepane![]() ![]() |
dichloromethane | N Param.: -3.80 sN Param.: 0.80 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
tri-p-tolylmethane (in MeCN)![]() ![]() |
MeCN | N Param.: -8.80 sN Param.: 0.82 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
bis(4-methoxyphenyl)phenylmethane (in MeCN)![]() ![]() |
MeCN | N Param.: -7.00 sN Param.: 0.82 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
tris(4-(dimethylamino)phenyl)methane (in MeCN)![]() ![]() |
MeCN | N Param.: -3.30 sN Param.: 0.82 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
bis(4-(dimethylamino)phenyl)phenylmethane (in MeCN)![]() ![]() |
MeCN | N Param.: -4.20 sN Param.: 0.82 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
10-methyl-9,10-dihydroacridine (in MeCN)![]() ![]() |
MeCN | N Param.: 4.00 sN Param.: 0.70 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
1,4-dihydronaphthalene (in MeCN)![]() ![]() |
MeCN | N Param.: -2.50 sN Param.: 1.00 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
1,2-dihydronaphthalene (in MeCN)![]() ![]() |
MeCN | N Param.: -3.30 sN Param.: 1.00 | ![]() | Chem. Eur. J. 2013, 19, 249-263 10.1002/chem.201202839 |
2-(trimethylsilyl)propene![]() ![]() |
dichloromethane | N Param.: -1.46 sN Param.: 1.05 | ![]() ![]() ![]() | Chem. Eur. J. 2014, 20, 1103-1110 10.1002/chem.201303215 |
2-(pentamethyldisilyl)propene![]() ![]() |
dichloromethane | N Param.: -0.26 sN Param.: 0.95 | ![]() ![]() ![]() | Chem. Eur. J. 2014, 20, 1103-1110 10.1002/chem.201303215 |
News
- 01/30/25:
Sesamol-derived ortho-quinone methides (o-QM) have been added (ChemEurJ 2024, e202403785 & OBC 2025, 23, 827-834) - 05/22/24:
Lactone enolates have been added (JOC 2024, 89, 6915-6928). - 11/13/24:
2-Methylene-1,2-dihydropyridines (2-pyNHOs) have been added (EurJOC 2024, 27, e202400373). - 05/21/24:
Mesoionic pyridinium-derived N-heterocyclic olefins (py-mNHOs) have been added (Angew. Chem. Int. Ed. 2024, 63, e202318283). - 10/19/23:
Enamines derived from 4-(alkylthio)-3-imidazolines and aldehydes have been added (ChemEurJ 2023, doi: 10.1002/chem.202302764). - 09/28/23:
Mesoionic N-heterocyclic olefins (mNHOs) have been added (Angew. Chem. Int. Ed. 2023, 62, e202309790). - 07/05/23:
S-Cyanomethylated imidazolidine-4-thione-derived enamines have been added (ChemComm 2023, 59, 8091). - 03/16/23:
Cyclic alpha-diazo carbonyl compounds added (EurJOC 2023, 26, e202300005) - 01/30/23:
NADH and NADPH reactivities (in water, pH 7) determined by Mayer and Moran have been added (OBC 2022, 21, 85-88). - 09/20/22:
Alkenyl boronate nucleophilicity by Liu, Ready and co-workers has been added (JACS 2022, 144, 16118). - 01/30/23:
Electrophilicities of diazo compounds in azo couplings (ChemEurJ 2022, 28, e202201376) - 01/30/23:
Diazocyclopentadiene added (Synthesis 2023, 55, 354-358) - 01/30/23:
Electrophilic indoles added (ChemCommun 2021, 57, 10071-10074) - 04/13/21:
Cyclic Michael acceptors added (Chem. Sci. 2021, 12, 4850-4865) - 05/21/21:
Thiophenolates (in DMSO) added (JOC 2021, 86, 5965-5972) - 05/06/20:
Heteroallenes added (JACS 2020, 142, 8383-8402). - 01/27/20:
Pyrrolidines and Imidazolidinones added (JACS 2020, 142, 1526-1547). - 05/06/20:
GSH reactivity added (Angew. Chem. Int. Ed. 2019, 58, 17704-17708) - 01/30/23:
Phenolates added (JOC 2019, 84, 8837-8858) - 04/24/18:
Ketones added (JACS 2018, 140, 5500). - 11/03/17:
Allyl-boron nucleophiles added (JACS 2017, 139, 15324) - 04/23/18:
Peroxide anions added (Angew. Chem. Int. Ed. 2017, 56, 13279). - 04/23/18:
Michael acceptors added (JACS 2017, 139, 13318). - 06/16/17:
Nucleophilicities of VNS reagents (JOC 2017, 82, 1011).