Selectivity Reversal during Thia-Michael Additions Using Tetrabutylammonium Hydroxide: Operationally Simple and Extremely High Turnover-Reference-Cited by-同舟云学术

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Selectivity Reversal during Thia-Michael Additions Using Tetrabutylammonium Hydroxide: Operationally Simple and Extremely High Turnover

Published:2014-04-11 Issue:13 Volume:46 Page:1725-1730
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Nicponski Daniel,Marchi Jennifer

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1341106.pdf

Cited by 14 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

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2. Alkylthialactonization: A novel protocol for access to either diastereoisomer of α-(thiomethyl)-γ-butyrolactones;Tetrahedron Letters;2023-07

3. Thia-Michael Reaction under Heterogeneous Catalysis;Organics;2023-02-21

4. One-pot synthesis of thioethers from indoles and p-quinone methides using thiourea as a sulfur source;Organic & Biomolecular Chemistry;2023

5. Metal-free thiolation of sulfonyl hydrazone with thiophenol: synthesis of 4-thio-chroman and diarylmethyl thioethers;Organic & Biomolecular Chemistry;2023

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