## 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
ChemInform Abstract: Diastereoselective Cyclopropanation of α,β-Unsaturated Acetals of a Novel Camphor-Derived Chiral Auxiliary.
✍ Scribed by Perry T. Kaye; Warner E. Molema
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Diastereoselective Cyclopropanation of α,β-Unsaturated Acetals of a Novel Camphor-Derived Chiral Auxiliary.
-2-exo-3-exo-Dihydroxybornane-10-sulfonate (III) proves to be a highly efficient chiral auxiliary for the asymmetric Simmons-Smith cyclopropanation of α,βunsaturated acetal derivatives [cf.
(V)→(VII)]. -(KAYE, PERRY T.;
📜 SIMILAR VOLUMES
## 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
Asymmetric Simmons-Smith Cyclopropanation of α,β-Unsaturated Bornane-2,3-diol Acetals. -Reaction of selected α,β-unsaturated aldehydes (II) with bornanediol (I) affords novel chiral acetals (III), which undergo diastereoselective cyclopropanation with a Simmons-Smith reagent giving compounds (V). -