Asymmetric synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates in 25-40% enantiomeric purities via the reaction of methyl (2Z)-3-aryl-2-(bromomethyl)prop-2-enoates with prop-2-yn-1-ol in the presence of quinidine is described
Treatment of piperazine with 3-acetoxy-2-methylenealkanenitriles provides exclusively (1,4)-bis[(2Z)...
The Baylis-Hillman reaction with chiral a-amino aldehydes has been revisited. The reaction carried o...
The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita–Baylis–Hillma...
A facile, simple and one-pot conversion of methyl 3-aryl-3-hydroxy-2-methylenepropanoates into methy...
Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substitute...
A simple synthesis of functionalized (1H)-quinol-2-ones and quinolines from the Baylis-Hillman adduc...
Reaction of methyl 3-acetoxy-2-methylenealkanoates with the reducing agent, lithium aluminium hydrid...
The bifunctional catalyst 6'-deoxy-6'-acylamino-beta -isocupreidine served both as a base to trigger...
In this doctoral thesis, the mechanism of the Lewis base-mediated aza-Baylis-Hillman reaction was ex...
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an...
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an...
MBH is an atom efficient reaction that provides densely functionalised adducts and generates a chira...
Thioureas straightforwardly derived from commercially available enantiopure amino alcohols have been...
The beta -isocupreidine (beta -ICD) or beta -ICD-amide (I)-catalyzed aza-Morita-Baylis-Hillman react...
Abstract: A methanolic ammonia-mediated alternate, easy and practical stereoselective synthesis of a...
Treatment of piperazine with 3-acetoxy-2-methylenealkanenitriles provides exclusively (1,4)-bis[(2Z)...
The Baylis-Hillman reaction with chiral a-amino aldehydes has been revisited. The reaction carried o...
The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita–Baylis–Hillma...
A facile, simple and one-pot conversion of methyl 3-aryl-3-hydroxy-2-methylenepropanoates into methy...
Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substitute...
A simple synthesis of functionalized (1H)-quinol-2-ones and quinolines from the Baylis-Hillman adduc...
Reaction of methyl 3-acetoxy-2-methylenealkanoates with the reducing agent, lithium aluminium hydrid...
The bifunctional catalyst 6'-deoxy-6'-acylamino-beta -isocupreidine served both as a base to trigger...
In this doctoral thesis, the mechanism of the Lewis base-mediated aza-Baylis-Hillman reaction was ex...
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an...
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an...
MBH is an atom efficient reaction that provides densely functionalised adducts and generates a chira...
Thioureas straightforwardly derived from commercially available enantiopure amino alcohols have been...
The beta -isocupreidine (beta -ICD) or beta -ICD-amide (I)-catalyzed aza-Morita-Baylis-Hillman react...
Abstract: A methanolic ammonia-mediated alternate, easy and practical stereoselective synthesis of a...
Treatment of piperazine with 3-acetoxy-2-methylenealkanenitriles provides exclusively (1,4)-bis[(2Z)...
The Baylis-Hillman reaction with chiral a-amino aldehydes has been revisited. The reaction carried o...
The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita–Baylis–Hillma...