KOH-catalyzed cross-coupling of primary and secondary alcohols: evidence for radical pathways

[1] Obora Y(2014)Recent advances in α-alkylation reactions using alcohols with hydrogen borrowing methodologies ACS Catal. 4 3972-undefined

[2] Satyanarayana P(2013)Tris(acetylacetonato) rhodium(III)-catalyzed α-alkylation of ketones, β-alkylation of secondary alcohols and alkylation of amines with primary alcohols Adv. Synth. Catal. 355 1859-undefined

[3] Reddy GM(2010)Cross-coupling reaction of alcohols for C-C bond formation using pincer type NHC/palladium catalysts Org. Biomol. Chem. 8 896-undefined

[4] Maheswaran H(2020)Room-temperature Guerbet reaction with unprecedented catalytic efficiency and enantioselectivity Angew. Chem. Int. Ed. 59 11384-undefined

[5] Kantam ML(2021)Nickel-catalyzed Guerbet type reaction: C-alkylation of secondary alcohols via double (de) hydrogenation Org. Lett. 23 3320-undefined

[6] Kose O(2020)KO Chem. Asian J. 15 518-undefined

[7] Saito S(2022)Bu-catalyzed Michael addition reactions under mild and solvent-free conditions J. Org. Chem. 87 6695-undefined

[8] Ng WT(2014)Base-catalyzed traceless silylation and deoxygenative cyclization of chalcones to cyclopropanes Angew. Chem. Int. Ed. 53 225-undefined

[9] Liao G(2021)Catalyst-free dehydrative a-alkylation of ketones with alcohols: Green and selective autocatalyzed synthesis of alcohols and ketones Chem Asian J. 16 3124-undefined

[10] Lau KK(2011)Selective C-alkylation between alcohols catalyzed by N-heterocyclic carbene molybdenum Chem. Eur. J. 17 9911-undefined

[1] Obora Y(2014)Recent advances in α-alkylation reactions using alcohols with hydrogen borrowing methodologies ACS Catal. 4 3972-undefined

[2] Satyanarayana P(2013)Tris(acetylacetonato) rhodium(III)-catalyzed α-alkylation of ketones, β-alkylation of secondary alcohols and alkylation of amines with primary alcohols Adv. Synth. Catal. 355 1859-undefined

[3] Reddy GM(2010)Cross-coupling reaction of alcohols for C-C bond formation using pincer type NHC/palladium catalysts Org. Biomol. Chem. 8 896-undefined

[4] Maheswaran H(2020)Room-temperature Guerbet reaction with unprecedented catalytic efficiency and enantioselectivity Angew. Chem. Int. Ed. 59 11384-undefined

[5] Kantam ML(2021)Nickel-catalyzed Guerbet type reaction: C-alkylation of secondary alcohols via double (de) hydrogenation Org. Lett. 23 3320-undefined

[6] Kose O(2020)KO Chem. Asian J. 15 518-undefined

[7] Saito S(2022)Bu-catalyzed Michael addition reactions under mild and solvent-free conditions J. Org. Chem. 87 6695-undefined

[8] Ng WT(2014)Base-catalyzed traceless silylation and deoxygenative cyclization of chalcones to cyclopropanes Angew. Chem. Int. Ed. 53 225-undefined

[9] Liao G(2021)Catalyst-free dehydrative a-alkylation of ketones with alcohols: Green and selective autocatalyzed synthesis of alcohols and ketones Chem Asian J. 16 3124-undefined

[10] Lau KK(2011)Selective C-alkylation between alcohols catalyzed by N-heterocyclic carbene molybdenum Chem. Eur. J. 17 9911-undefined