## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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
Neutral and ionic reaction mechanisms for the allylation of aldehydes by bipyridine N,N′-dioxides
✍ Scribed by Hrdina, Radim; Opekar, František; Roithová, Jana; Kotora, Martin
- Book ID
- 120850507
- Publisher
- Royal Society of Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 607 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1359-7345
- DOI
- 10.1039/B819545E
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## Abstract magnified image Unsymmetrically 3,3′‐substituted axially chiral bis(tetrahydroisoquinoline) __N,N′‐__dioxides can be prepared in just three steps. They exhibit unique catalytic activity (turnover frequency, enantioselectivity, substrate scope) in the asymmetric allylation of aromatic a
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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
## Abstract Palladium‐catalyzed cross‐coupling of bipyridine __N,N′__‐dioxide 6,6′‐dichloride (__R__~__nap__~__,R__~__pyr__~)‐**1** with the aryl Grignard reagents opened a new approach to axially chiral bipyridine __N,N′‐__dioxides (__R__)‐**2** bearing a variety of aryl groups at the 6 and 6′ pos