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Book ChapterDOI

Thiopyrans and Their Benzo Derivatives

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The article was published on 2020-01-01. It has received 1 citations till now. The article focuses on the topics: Ring (chemistry) & Section (typography).

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Journal ArticleDOI

Organocatalytic and electrophilic approach to oxindoles with C3-quaternary stereocenters.

TL;DR: A Lewis base-catalyzed asymmetric allylic alkylation of Morita-Baylis-Hillman carbonates derived from isatins has been investigated, which provides an electrophilic pathway to access oxindoles bearing C3-quaternary stereocenters.
Journal ArticleDOI

A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric anti-selective Mannich reactions and syn-selective cross-aldol reactions.

TL;DR: A direct asymmetric Mannich reaction using a novel axially chiral amino sulfonamide (S)-3 that is highly anti- and enantioselective has been developed and has also been successfully applied to asymmetric direct cross-aldol reaction between two different aldehydes.
Journal ArticleDOI

Molecular design of deep blue fluorescent emitters with 20% external quantum efficiency and narrow emission spectrum

TL;DR: A thermally activated delayed fluorescent (TADF) emitter using a rigid 9,9-dimethyl-9H-thioxanthene 10,10-dioxide (DMTD) acceptor and an acridine donor was developed in this article.
Journal ArticleDOI

Organocatalytic asymmetric intermolecular dehydrogenative α-alkylation of aldehydes using molecular oxygen as oxidant.

TL;DR: An organocatalytic enantioselective intermolecular oxidative dehydrogenative α-alkylation of aldehydes via benzylic C-H bond activation has been developed using simple and green molecular oxygen as the oxidant.
Journal ArticleDOI

Synthesis of 2,3,4-Trisubstituted Thiochromanes using an Organocatalytic Enantioselective Tandem Michael-Henry Reaction.

TL;DR: Enantioenriched 2,3,4-trisubstituted thiochromanes have been synthesized by using a cupreine-catalyzed tandem Michael addition-Henry reaction between 2-mercaptobenzaldehydes and β-nitrostyrenes.