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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


ChemInform Abstract: Diastereoselective
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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 “Full Text” option. The original article is trackable v

ChemInform Abstract: Diastereoselective
✍ Kung-Shuo Yang; Kwunmin Chen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

## 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: Asymmetric Simmons—
✍ Perry T. Kaye; Warner E. Molema 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

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). -