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ChemInform Abstract: Asymmetric Methoxyselenenylations with Camphor-Based Selenium Electrophiles.

✍ 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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✦ 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,


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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 β€œFull Text” option. The original article is trackable v