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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

A Rational Approach towards the Nucleophilic Substitutions of Alcohols “on Water”

TL;DR: The direct substitution of alcohols “on water” without added Brønsted or Lewis acid is possible; the reaction is related to the stability of the corresponding carbocation, and the lifetimes of carbocations can be increased substantially by the introduction of electron-donating substituents on the aryl ring.
Journal ArticleDOI

Decarboxylative Trifluoromethylation of Aliphatic Carboxylic Acids

TL;DR: An efficient method for the conversion of carboxylic acids to trifluoromethyl groups via the combination of photoredox and copper catalysis is disclosed, which tolerates a wide range of functionality including heterocycles, olefins, alcohols, and strained ring systems.
Journal ArticleDOI

Dual Organocatalysis: Asymmetric Allylic–Allylic Alkylation of α,α‐Dicyanoalkenes and Morita–Baylis–Hillman Carbonates

TL;DR: The first highly enantioselective allylic-allylic alkylation of alpha,alpha-dicyanoalkenes and Morita-Baylis-Hillman carbonates by dual catalysis of (DHQD)(2)AQN and (S)-BINOL has been investigated.
Journal ArticleDOI

Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes.

TL;DR: A highly enantioselective intramolecular Stetter reaction of aromatic and aliphatic aldehydes tethered to different Michael acceptors has been developed and the substrate scope has been examined and found to be broad.
Journal ArticleDOI

A single component ratiometric pH probe with long wavelength excitation of europium emission

TL;DR: Following excitation in therange 370-405 nm, the emission spectrum of a cell permeable macrocyclic Eu(III) complex incorporating an N-methylsulfonamide moiety changes form with pH, allowing ratiometric pH measurements in the range 6 to 8.