Mechanism and Regioselectivity of the Cycloaddition of Thiones Derived from Meldrum’s Acid, Malonates, or Other Dicarbonyls-Reference-Cited by-同舟云学术

Mechanism and Regioselectivity of the Cycloaddition of Thiones Derived from Meldrum’s Acid, Malonates, or Other Dicarbonyls

Published:2008-09-05 Issue:19 Volume:73 Page:7457-7466
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Perreault Stéphane¹,Poirier Maude¹,Léveillé Pascal¹,René Olivier¹,Joly Pascal¹,Dory Yves¹,Spino Claude¹

Affiliation:

1. Département de Chimie, Université de Sherbrooke, 2500 Boul. Université, Sherbrooke, QC, Canada J1K 2R1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800945y

Reference47 articles.

1. aBoger, D. L.; Weinreb, S. M.InHetero Diels−Alder Methodology in Organic Synthesis;Wasserman, H. H., Ed.Academic Press Inc.: San Diego, 1987; Organic Chemistry, a Series Monograph, Vol.47, pp120−145.

2. Synthetic aspects of diels-alder cycloadditions with heterodienophiles

3. The Use of Thiocarbonyl Compounds in Carbon-Carbon Bond Forming Reactions

4. A Thio-Diels−Alder Route to the Azocine Ring System. Total Synthesis of (±)-Otonecine

5. Meldrum's Acid-Derived Thione Dienophile in a Convergent and Stereoselective Synthesis of a Tetracyclic Quassinoid Intermediate

Cited by 12 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. Unveiling [3 + 2] cycloaddition reactions of diphenyl diazomethane to thiobenzophenone and cycloaliphatic thioketones in the light of molecular electron density theory;Computational and Theoretical Chemistry;2024-07

2. Thiiranes and Thiirenes: Monocyclic;Comprehensive Heterocyclic Chemistry IV;2022

3. Thiopyrans and Their Benzo Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

4. Selected applications of Meldrum's acid – a tutorial;Organic & Biomolecular Chemistry;2021

5. A Unique (3+2) Annulation Reaction between Meldrum's Acid and Nitrones: Mechanistic Insight by ESI-IMS-MS and DFT Studies;Chemistry - A European Journal;2018-02-15