The first α-alkylation of α,β,γ,δ-unsaturated aldehydes is achieved under mild reaction conditions. Several α,β,γ,δ-unsaturated aldehydes and diarylcarbinols are successfully tested for the synthesis of MBH-type α-alkylated products with an excellent regioselectivity. Simple pyrrolidine is efficiently used as a catalyst to achieve a perfect E/Z selectivity of the α-alkylated products.by Venkata M. D Padmaja,, Sachin Jangra and Chandrakumar Appaye
Trichloromethyl carbinols have been used for over a century to afford α-substituted carboxylic ...
This thesis deals with the development and application of new synthetic methodology for stereo- or r...
Thesis (Ph. D.)--University of Rochester. Department of Chemistry, 2016.Part I. Mechanistic Studies,...
Selectively alkylating an alpha beta unsaturated aldehyde at gamma position has been a challenging ...
Based on a modification of the Doebner–Knoevenagel reaction, a practical and highly efficient synthe...
The 1,4-elimination reaction of (Z)-N-Boc-2-(4-methoxy-2-alkenyloxy)pyrrolidines (1) is shown to pro...
Formaldehyde is used as a one-carbon electrophile(1) in several organic transformations to functiona...
The regioselective alkylation of an oxonaphthalene-annelated pyrrole system is reported. The regiose...
α,β-Unsaturated aldehydes are conveniently prepared from ketones through their β-diethoxymethyl deri...
The enantioselective allylation of ketones represents both a problem of fundamental importance in as...
The 1,4-elimination reaction of 2-substituted-(2Z)-4-methoxy-O-alkenyl acetals with n-butyllithium i...
A practical and high yielding synthesis of α,β-unsaturated esters from aldehydes and 1,1-diethoxyeth...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
AbstractReactions of N-alkyl-2,3-dihydro-4-pyridones and 4-(pyrrolidin-1-yl)furan-2(5H)-one with ald...
α-Methoxy- and α-ethoxyketones, as important intermediates in organic synthesis and flavor compounds...
Trichloromethyl carbinols have been used for over a century to afford α-substituted carboxylic ...
This thesis deals with the development and application of new synthetic methodology for stereo- or r...
Thesis (Ph. D.)--University of Rochester. Department of Chemistry, 2016.Part I. Mechanistic Studies,...
Selectively alkylating an alpha beta unsaturated aldehyde at gamma position has been a challenging ...
Based on a modification of the Doebner–Knoevenagel reaction, a practical and highly efficient synthe...
The 1,4-elimination reaction of (Z)-N-Boc-2-(4-methoxy-2-alkenyloxy)pyrrolidines (1) is shown to pro...
Formaldehyde is used as a one-carbon electrophile(1) in several organic transformations to functiona...
The regioselective alkylation of an oxonaphthalene-annelated pyrrole system is reported. The regiose...
α,β-Unsaturated aldehydes are conveniently prepared from ketones through their β-diethoxymethyl deri...
The enantioselective allylation of ketones represents both a problem of fundamental importance in as...
The 1,4-elimination reaction of 2-substituted-(2Z)-4-methoxy-O-alkenyl acetals with n-butyllithium i...
A practical and high yielding synthesis of α,β-unsaturated esters from aldehydes and 1,1-diethoxyeth...
Functionalization of carbonyl compounds has been intensively studied for a long time as carbonyl com...
AbstractReactions of N-alkyl-2,3-dihydro-4-pyridones and 4-(pyrrolidin-1-yl)furan-2(5H)-one with ald...
α-Methoxy- and α-ethoxyketones, as important intermediates in organic synthesis and flavor compounds...
Trichloromethyl carbinols have been used for over a century to afford α-substituted carboxylic ...
This thesis deals with the development and application of new synthetic methodology for stereo- or r...
Thesis (Ph. D.)--University of Rochester. Department of Chemistry, 2016.Part I. Mechanistic Studies,...