Collect. Czech. Chem. Commun.
2005, 70, 1953-1969
https://doi.org/10.1135/cccc20051953
Sulfoxide-Modified Julia-Lythgoe Olefination: Highly Stereoselective Di-, Tri-, and Tetrasubstituted Double Bond Formation
Jiří Pospíšil, Tomáš Pospíšil and István E. Markó*
Département de Chimie, Université catholique de Louvain, Place Louis Pasteur 1, B-1348 Louvain-la-Neuve, Belgium
Crossref Cited-by Linking
- Varsha Vijayan, Radhika Sankaran, Anilkumar Gopinathan: An Overview of Julia-lythgoe Olefination. COS 2024, 21, 97. <https://doi.org/10.2174/1570179420666230510104114>
- Zhu Shihao, Yu Chunmian, Shi Wenjun, Zhou Xinrui: Selective and mild sulfoxidation of 2-sulfylbenzothiazole using hydroperoxides derived from cyclohexanone in the absence of catalyst. Tetrahedron 2021, 90, 132203. <https://doi.org/10.1016/j.tet.2021.132203>
- Chatterjee Bhaskar, Bera Smritilekha, Mondal Dhananjoy: Julia–Kocienski olefination: a key reaction for the synthesis of macrolides. Tetrahedron: Asymmetry 2014, 25, 1. <https://doi.org/10.1016/j.tetasy.2013.09.027>
- Pospíšil Jiří, Markó István E.: Metathesis-based synthesis of 3-methoxy α,β-unsaturated lactones: total synthesis of (R)-kavain and of the C1–C6 fragment of jerangolid D. Tetrahetron Lett 2008, 49, 1523. <https://doi.org/10.1016/j.tetlet.2007.12.113>
- Pospisil Jiri, Pospisil Tomas, Marko Istvan E.: Sulfoxide‐Modified Julia—Lythgoe Olefination: Highly Stereoselective Di‐, Tri‐, and Tetrasubstituted Double Bond Formation. ChemInform 2006, 37. <https://doi.org/10.1002/chin.200620051>
- Pospíšil Jiří, Markó István E.: Total synthesis of (R)-(+)-goniothalamin and (R)-(+)-goniothalamin oxide: first application of the sulfoxide-modified Julia olefination in total synthesis. Tetrahetron Lett 2006, 47, 5933. <https://doi.org/10.1016/j.tetlet.2006.06.054>
- Pospíšil Jiří, Markó István E.: Efficient and Stereoselective Synthesis of Allylic Ethers and Alcohols. Org. Lett. 2006, 8, 5983. <https://doi.org/10.1021/ol062433y>
