Arjun Gontala | Savitribai Phule Pune University (original) (raw)
Papers by Arjun Gontala
Asian Journal of Organic Chemistry, Oct 20, 2015
A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxi... more A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxidative ring-opening of epoxides with aromatic aldehydes is described. This regioselective, oxidative process utilizes a N-bromosuccinimide (NBS)/DMSO combination as the oxidant system and Et3N as the base under mild reaction conditions.
Organic Letters, Dec 23, 2022
Bulletin of the Korean Chemical Society, 2021
Advanced Synthesis & Catalysis, 2020
Asian Journal of Organic Chemistry, 2015
A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxi... more A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxidative ring-opening of epoxides with aromatic aldehydes is described. This regioselective, oxidative process utilizes a N-bromosuccinimide (NBS)/DMSO combination as the oxidant system and Et3N as the base under mild reaction conditions.
European Journal of Organic Chemistry, 2016
Asian Journal of Organic Chemistry, Oct 20, 2015
A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxi... more A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxidative ring-opening of epoxides with aromatic aldehydes is described. This regioselective, oxidative process utilizes a N-bromosuccinimide (NBS)/DMSO combination as the oxidant system and Et3N as the base under mild reaction conditions.
Organic Letters, Dec 23, 2022
Bulletin of the Korean Chemical Society, 2021
Advanced Synthesis & Catalysis, 2020
Asian Journal of Organic Chemistry, 2015
A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxi... more A high-yielding synthesis of α-acyloxyketones using a N-heterocyclic-carbene (NHC)-catalyzed, oxidative ring-opening of epoxides with aromatic aldehydes is described. This regioselective, oxidative process utilizes a N-bromosuccinimide (NBS)/DMSO combination as the oxidant system and Et3N as the base under mild reaction conditions.
European Journal of Organic Chemistry, 2016