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ChemInform Abstract: Mg-Promoted Reductive Cross Coupling of Carbonyl Compounds with Trimethylsilyl Chloride.

โœ Scribed by Y. ISHINO; H. MAEKAWA; H. TAKEUCHI; K. SUKATA; I. NISHIGUCHI

Book ID
112027022
Publisher
John Wiley and Sons
Year
2010
Weight
28 KB
Volume
27
Category
Article
ISSN
0931-7597

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Mg-Promoted Reductive Coupling of Aromat
Mg-Promoted Reductive Coupling of Aromatic Carbonyl Compounds with Trimethylsilyl Chloride and Bis(chlorodimethylsilyl) Compounds.
โœ Tetsuro Uchida; Yoshio Kita; Hirofumi Maekawa; Ikuzo Nishiguchi ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons โš– 30 KB ๐Ÿ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Facile synthesis of silyl enol ethers by
Facile synthesis of silyl enol ethers by Mg-promoted coupling of aliphatic carbonyl compounds with trimethylsilyl chloride
โœ Yoshio Ishino; Yoshio Kita; Hirofumi Maekawa; Toshinobu Ohno; Yasuhiro Yamasaki; ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 225 KB

Treatment of aliphatic carbonyl compounds with trimethyisilyl chloride with Mg turning for Grignard reaction without any pre-treatmem in N,N-dimethylformamide at room temperature brought about highly facile, effective and stereoselective coupling to give the corresponding silyl enol ethers in good y