Epoxides: Small rings to play with under asymmetric organocatalysis

S Meninno, A Lattanzi - ACS Organic & Inorganic Au, 2022 - ACS Publications
Optically pure epoxides are recognized as highly valuable products and key intermediates,
useful in different areas from pharmaceutical and agrochemical industries to natural product …

Biocatalytic thionation of epoxides for enantioselective synthesis of thiiranes

R Ma, X Hua, CL He, HH Wang, ZX Wang… - Angewandte …, 2022 - Wiley Online Library
Expanding the enzymatic toolbox for the green synthesis of valuable molecules is still of
high interest in synthetic chemistry and the pharmaceutical industry. Chiral thiiranes are …

Thiocarbonyl surrogate via combination of sulfur and chloroform for thiocarbamide and oxazolidinethione construction

W Tan, J Wei, X Jiang - Organic letters, 2017 - ACS Publications
An efficient and practical thiocarbonyl surrogate via combination of sulfur and chloroform
has been developed. A variety of thiocarbamides and oxazolidinethiones have been …

One-Pot Synthesis of Furo[3,4-c]indolo[2,1-a]isoquinolines through Rh(III)-Catalyzed Cascade Reactions of 2-Phenylindoles with 4-Hydroxy-2-alkynoates

Y Liu, Z Yang, R Chauvin, W Fu, Z Yao, L Wang… - Organic …, 2020 - ACS Publications
An efficient and regioselective synthesis of fused polycyclic furo [3, 4-c] indolo [2, 1-a]
isoquinolines through Rh (III)-catalyzed cascade C–H activation/annulation/lactonization of …

Palladium‐Catalyzed Oxygenative Cross‐Coupling of Ynamides and Benzyl Bromides by Carbene Migratory Insertion

Y Gao, G Wu, Q Zhou, J Wang - … Chemie International Edition, 2018 - Wiley Online Library
A palladium‐catalyzed oxygenative cross‐coupling of ynamides and benzyl bromides has
been developed. After subsequent hydrogenation, α, α‐disubstituted amide derivatives were …

Catalytic Enantioselective Synthesis of Tertiary Thiols From 5H‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis

S Diosdado, J Etxabe, J Izquierdo… - Angewandte Chemie …, 2013 - Wiley Online Library
The direct catalytic reaction between an enolizable carbonyl compound and an electrophile
under proton-transfer conditions has emerged as a challenging versatile transformation in …

Asymmetric catalytic (2+ 1) cycloaddition of thioketones to synthesize tetrasubstituted thiiranes

X Lin, M Pu, X Sang, S Li, X Liu… - Angewandte Chemie …, 2022 - Wiley Online Library
Herein, we report the first example of enantioselective (2+ 1) cycloaddition of thioketones
with α‐diazo pyrazoleamides for the direct synthesis of tetrasubstituted thiiranes. In the …

Synthesis of cis-thiiranes as diastereoselective access to epoxide congeners via 4π-electrocyclization of thiocarbonyl ylides

S Song, J Jin, JH Choi, W Chung - Nature Communications, 2022 - nature.com
Organochalcogen heterocycles are ubiquitously present and widely utilized in various fields.
Among them, oxirane has been extensively studied, and all of the stereoisomeric forms are …

Catalyst‐Controlled Stereoselective Barton–Kellogg Olefination

TA Schmidt, C Sparr - Angewandte Chemie International …, 2021 - Wiley Online Library
Overcrowded alkenes are expeditiously prepared by the versatile Barton–Kellogg
olefination and have remarkable applications as functional molecules owing to their unique …

Catalytic enantioselective conversion of epoxides to thiiranes

S Liao, M Leutzsch, MR Monaco… - Journal of the American …, 2016 - ACS Publications
A highly efficient and enantioselective Brønsted acid catalyzed conversion of epoxides to
thiiranes has been developed. The reaction proceeds in a kinetic resolution, furnishing both …