Cp2TiC12 -CATALYZED REACTION OF GRIGNARD REAGENTS WITH ISOCYANATES, FORMATION OF REDUCTION-COUPLING PRODUCT OF ISOCYANATES\*
β¦ LIBER β¦
Cp2TiCl2-Catalyzed reaction of grignard reagents with isocyanates, formation of carboxamide with rearranged carbonskeleton
β Scribed by Yongmin Zhang; Jinlong Jiang; Yongqian Chen
- Book ID
- 104227785
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 150 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Isocyanates react with isopropyl or set-butylmagnesium bromide in the presence of a small amount of Cp2TiCl to afford amide5 with normal alkyl group.
A possibl mechanism for this reac 3 ion is proposed.
Cp2TiC12 has recently received more and more attention in organic synthesis.
Sato and his co-workers have reported
Cp2TiCl2-catalyzed reaction of Grignard reagents with several kinds of organic substrates 1 . Recently we also described
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