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Stereoselective Simmons—Smith Cyclopropanation of Chiral Enamides.

✍ Scribed by Zhenlei Song; Ting Lu; Richard P. Hsung; Ziyad F. Al-Rashid; Changhong Ko; Yu Tang

Publisher
John Wiley and Sons
Year
2007
Weight
35 KB
Volume
38
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

Stereoselective Simmons–Smith Cyclopropa
Stereoselective Simmons–Smith Cyclopropanation of Chiral Enamides
✍ Zhenlei Song; Ting Lu; Richard P. Hsung; Ziyad F. Al-Rashid; Changhong Ko; Yu Ta 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 160 KB 👁 1 views

hsungGroup/ [\*\*] We thank NIH-NIGMS (GM066055) and UW-Madison for financial support. We also thank Ben Kucera and Vic Young for solving the X-ray crystal structures.

ChemInform Abstract: Asymmetric Simmons—
ChemInform Abstract: Asymmetric Simmons—Smith Cyclopropanation of α,β-Unsaturated Bornane-2,3-diol Acetals.
✍ Perry T. Kaye; Warner E. Molema 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

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). -