Ni-catalyzed ring-opening reactions of alkyl-substituted cyclopropanes; role of unreduced Ni species
✍ Scribed by István Pálinkó; Ferenc Notheisz; Mihály Bartók
- Publisher
- Elsevier Science
- Year
- 1991
- Weight
- 404 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0304-5102
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
a-Lithiated 1-[(2-methoxyethoxy)methoxy]-2-(phenylsylfinyl)cyclopropane reacted smoothly with alkylating agents to afford the corresponding a-alkylated cyclopropylsulfoxides, which underwent the Pummerer-type reaction mediated ring-opening at low temperature (-78°C) by employing TFAA/Pr i 2 NEt/CH 2
## 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