## 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, please click on HTML or PDF.
Chiral Version of the Burgess Reagent and Its Reactions with Oxiranes: Application to the Formal Enantiodivergent Synthesis of Balanol †
✍ Scribed by Sullivan, Bradford; Gilmet, Jacqueline; Leisch, Hannes; Hudlicky, Tomas
- Book ID
- 127166818
- Publisher
- American Chemical Society
- Year
- 2008
- Tongue
- English
- Weight
- 121 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0163-3864
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Treatment of optically active 2,3-epoxyalcohols with trialkylaluminum reagents followed by periodate cleavage constitutes a convenient synthesis of a-chiral aldehyde derivatives, especially when the branching alkyl group is methyl. We recently required a convenient source of either 1,2-diol 2 or 1,3
The cross-coupling reaction of orqanozinc chlorides with (Z)-2bromo-1-alkenylboranes prepared by the bromoboration reaction of 1-alkynes with tribromoborane, proceeds in the presence of a palladium catalyst to give 2,2\_disubstituted alkenylboranes, which can be used for the di-or trisubstituted alk