85683-79-0Relevant academic research and scientific papers
Organocatalytic Isomerization/Allylic Alkylation of O-Acylated Hemithioacetals and Their Application in Tandem Sequence to Access 2,7-Dioxabicyclo[2.2.1]heptan-3-one Derivatives
Zhang, Huan-Qing,Xi, Ji-Ming,Liao, Wei-Wei
, p. 1168 - 1180 (2020/01/31)
A novel protocol for the efficient preparation of α-hydroxy allylic thioesters via a Lewis base-catalyzed tandem isomerization/allylic alkylation process is reported. The resulting allylic thioesters can serve as valuable scaffolds to undergo a stereosele
Pummerer reaction of sulfoxides in acetic anhydride catalyzed by Al-MCM-41
Ito, Suguru,Kubota, Yoshihiro,Asami, Masatoshi
, p. 16 - 18 (2016/01/20)
The Pummerer reaction of acetic anhydride with both alkyl aryl sulfoxides and dialkyl sulfoxides was efficiently promoted by a mesoporous aluminosilicate Al-MCM-41 to afford the corresponding α-acetoxy sulfides in high yields. The catalyst was easily reco
Organocatalytic asymmetric tandem condensation-intramolecular rearrangement-protonation: An approach to optically active α-amino thioester derivatives
Capitta, Francesca,Frongia, Angelo,Piras, Pier Paolo,Pitzanti, Patrizia,Secci, Francesco
supporting information; experimental part, p. 490 - 494 (2012/01/15)
An unprecedented and conceptually novel chiral Bronsted base/Bronsted acid catalytic method for the enantioselective synthesis of α-amino thioesters through a tandem condensation-intramolecular rearrangement-protonation has been developed which provides a number of important synthetic building blocks in good yield and with moderate to good enantioselectivities.
Enantioselective organocatalytic rearrangement of α-acyloxy- β-keto sulfides to α-acyloxy thioesters
Capitta, Francesca,Frongia, Angelo,Piras, Pier Paolo,Pitzanti, Patrizia,Secci, Francesco
supporting information; experimental part, p. 2955 - 2960 (2011/02/22)
The first highly enantioselective organocatalytic rearrangement of α-acyloxy-β-keto sulfides to α-acyloxy thioesters has been developed which provides a number of important synthetic building blocks in high yield and with excellent enantioselectivities (e
