Synthesis of stereochemically-biased spiropyrans by microwave-promoted, one-pot alkylation–condensation

Author:

Perry Alexis1234ORCID,Davis Kane1234ORCID,West Lara1234

Affiliation:

1. Biosciences

2. University of Exeter

3. Exeter EX4 4QD

4. UK

Abstract

Stereochemical control of spiropyran ring-closure was explored through synthesis of sterically-congested spiropyrans by a novel, efficient method.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. 5′-Substituted Indoline Spiropyrans: Synthesis and Applications;Colorants;2023-06-05

2. A Modern Look at Spiropyrans: From Single Molecules to Smart Materials;Topics in Current Chemistry;2023-01-10

3. Three Complementary One‐Pot Four‐Component Reaction Sequences for Rapid, General and Direct Spiropyran Synthesis;European Journal of Organic Chemistry;2022-12-08

4. Pyrans and Their Benzo Derivatives: Structure and Reactivity;Comprehensive Heterocyclic Chemistry IV;2022

5. Microwave Synthesized Functional Dyes;Microwave Heating - Electromagnetic Fields Causing Thermal and Non-Thermal Effects;2021-08-18

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