Conversion of 1-Boc-indoles to 1-Boc-oxindoles.
β Scribed by Enrique Vazquez; Joseph F. Payack
- Book ID
- 101961313
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 15 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
A new stereoselective synthesis of enantiomerically pure l-naphthylglycine has been developed. The source of chirality is the catalytic Sharpless epoxidation. Regioselective and stereospecific ring-opening of the corresponding epoxy alcohol is performed either with sodium azide or with benzhydrylami
Lewis Acid-mediated coupling reactions of (5R, 6S)-2-acetoxy-4-(benzyloxycarbonyl)-5,6-diphenyl-2,3,5,6-tetrahydro-4H-1,4-oxazine (2a) with aUylsilanes (3a-d) proceeded to give the coupling products (4a-b) with moderate to good stereoselectivity. The coupling products (4a-b) were effectively convert