18516-16-0Relevant academic research and scientific papers
Synthesis of quaternary carbon centers via hydroformylation
Sun,Frimpong,Tan
supporting information; experimental part, p. 11841 - 11843 (2010/11/04)
The application of hydroformylation to the synthesis of quaternary carbon centers is reported. The synthesis of the highly substituted carbon is achieved by applying a catalytic amount of 1. Ligand 1 serves as a catalytic directing group by covalently and reversibly binding to both the substrate and catalyst. The intramolecular nature of the directing group strategy accelerates the hydroformylation reaction such that the reaction is performed at mild temperatures (35-55 °C) and with excellent regioselectivity (b:l > 94:6).
A convenient one-pot synthesis of 2,2-dialkyl-2,3-dihydro-1H-naphtho[2,1-b] pyrans
Jha, Amitabh,Huang, Po-Jung Jimmy,Mukherjee, Chandrani,Paul, Nawal K.
, p. 3127 - 3130 (2008/09/19)
This work describes a convenient one-pot procedure for the synthesis of 2,2-disubstituted 2,3-dihydro-177-naphtho[2,1-b]pyrans {i.e. 2,2-disubstituted 1H-benzo[f]chromans} by the reaction of 2-tetralones and α,α- disubstituted β-hydroxy propionaldehydes under acidic conditions. Georg Thieme Verlag Stuttgart.
A Novel Synthesis of 14-(Hydroxymethylalkyl) Derivatives of Dibenzoxanthenes and 3,3-Dimethyl-4-(2-hydroxy-1-naphthyl)benzochroman
Sirkecioglu, Okan,Tahnh, Naciye,Akar, Ahmet
, p. 456 - 460 (2007/10/03)
Several reactions of 2-naphthol with 2-alkyl-2-hydroxymethylaldehydes have been investigated.Novel synthesis of 14-(hydroxymethyl)alkyldibenzoxanthenes and 3,3-dimethyl-4-(2-hydroxy-1-naphthyl)benzochroman has been realized.
