The alkylidene carbene generated by chloromethylenation / or-elimination of 1 proceeds with a high degree of selectivity for methoxy C-H insertion over methine insertion, to give 2. The carbene generated with trimethylsilyldiazomethane results in an approximately 1:1 mixture of 2 and 3.
✦ LIBER ✦
Diastereoselectivity in uncatalyzed intramolecular CH insertion by an alkylidene carbene
✍ Scribed by Douglass F. Taber; Robert P. Meagley
- Book ID
- 103402222
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 126 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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## 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
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