International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typical bielectrophile-binucleophile reaction that produces quaternary centers in a stereoselective manner, give access to Meyers’ chiral lactams in good yield and high diastereoselectivity in short times
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
A straightforward stereoselective and enantiodivergent cyclization strategy for the construction of ...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceHighly atroposelective Meyers' lactamization promoted by pivalic acid under mi...
International audienceHighly atroposelective Meyers' lactamization promoted by pivalic acid under mi...
International audienceA stereoselective approach to the preparation of 7,5-fused bicyclic lactams ba...
International audienceA stereoselective approach to the preparation of 7,5-fused bicyclic lactams ba...
Highly atroposelective Meyers’ lactamization promoted by pivalic acid under microwave irradiation is...
Highly atroposelective Meyers’ lactamization promoted by pivalic acid under microwave irradiation is...
An array of structurally diverse amides was synthesized efficiently by combining (primary and second...
Efficient synthesis of 1,2-disubstituted homochiral pyrroles has been achieved by a two-component co...
A microwave-promoted three-step tandem process for the synthesis of bicyclic γ-lactams is developed....
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
A straightforward stereoselective and enantiodivergent cyclization strategy for the construction of ...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceMicrowave solvent-free conditions developed for Meyers’ lactamization, a typic...
International audienceHighly atroposelective Meyers' lactamization promoted by pivalic acid under mi...
International audienceHighly atroposelective Meyers' lactamization promoted by pivalic acid under mi...
International audienceA stereoselective approach to the preparation of 7,5-fused bicyclic lactams ba...
International audienceA stereoselective approach to the preparation of 7,5-fused bicyclic lactams ba...
Highly atroposelective Meyers’ lactamization promoted by pivalic acid under microwave irradiation is...
Highly atroposelective Meyers’ lactamization promoted by pivalic acid under microwave irradiation is...
An array of structurally diverse amides was synthesized efficiently by combining (primary and second...
Efficient synthesis of 1,2-disubstituted homochiral pyrroles has been achieved by a two-component co...
A microwave-promoted three-step tandem process for the synthesis of bicyclic γ-lactams is developed....
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
Department of Chemistry, Faculty of Engineering & Technology, Veer Bahadur Singh Purvanchal Universi...
A straightforward stereoselective and enantiodivergent cyclization strategy for the construction of ...
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