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Chiral o-Methoxyaryldiazaphosphonamides − A New Class of Efficient Lewis Bases in the Catalytic Asymmetric Ring Opening of Cyclooctene Oxide with Silicon Tetrachloride

✍ Scribed by Gérard Buono

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
127 KB
Volume
2002
Category
Article
ISSN
1434-193X

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Chiral o-Methoxyaryldiazaphosphonamides
Chiral o-Methoxyaryldiazaphosphonamides − A New Class of Efficient Lewis Bases in the Catalytic Asymmetric Ring Opening of Cyclooctene Oxide with Silicon Tetrachloride
✍ Gérard Buono 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 84 KB 👁 1 views

This paper reported a new class of diastereomerically pure ortho-methoxydiazaphosphonamide Lewis bases prepared from the corresponding o-hydroxyarylphosphonamides. These bases have been applied to the catalytic asymmetric ring opening of cyclooctene oxide with SiCl 4 . During the last weeks, I discl

ChemInform Abstract: Chiral o-Methoxyary
ChemInform Abstract: Chiral o-Methoxyaryldiazaphosphonamides — A New Class of Efficient Lewis Bases in the Catalytic Asymmetric Ring Opening of Cyclooctene Oxide with Silicon Tetrachloride.
✍ Sebastien Reymond; Olivier Legrand; Jean Michel Brunel; Gerard Buono 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v