ChemInform Abstract: Asymmetric Methoxyselenenylations with Camphor-Based Selenium Electrophiles.
β Scribed by T. G. BACK; S. NAN
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
1999 organo-selenium compounds, isocyclic C derivatives organo-selenium compounds, isocyclic C derivatives S 0134
07 -189
Asymmetric Methoxyselenenylations with Camphor-Based Selenium Electrophiles.
-Asymmetric methoxyselenenylation of olefins is achieved by reaction with freshly prepared camphor-based selenenyl triflates (II) or (XI). The 2-oxo analogue (II) proves to be the most effective reactant. -(BACK,
π SIMILAR VOLUMES
1998 organo-selenium compounds, isocyclic C derivatives organo-selenium compounds, isocyclic C derivatives S 0134 15 -187 Asymmetric Methoxyselenenylation of Alkenes with Chiral Ferrocenylselenium Reagents. -Best results are observed using the ferrocenylselenium compound shown in the scheme. From c
## 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 βFull Textβ option. The original article is trackable v