N-Benzyl-2-deoxyxylonolactams are accessible by highly chemoselective, diastereoselective, and enantioselective carbon-hydrogen insertion reactions of diazoacetamides. Competing aromatic cycloaddition or b-lactam formation via carbon-hydrogen insertion into a benzylic position can be minimized by th
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ChemInform Abstract: An Enantioselective 1,2-Aziridinomitosene Synthesis via a Chemoselective Carbon—Hydrogen Insertion Reaction of a Metal Carbene.
✍ Scribed by Sangku Lee; Wai-Man Lee; Gary A. Sulikowski
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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