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Lewis Acid Mediated Addition of Silyl Ketene Acetals to Sulfinimines

✍ Scribed by Kawecki, Robert

Book ID: 126789516
Publisher: American Chemical Society
Year: 1999
Tongue: English
Weight: 98 KB
Volume: 64
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo990913f

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📜 SIMILAR VOLUMES

ChemInform Abstract: Lewis Acid Mediated

ChemInform Abstract: Lewis Acid Mediated Addition of Silyl Ketene Acetals to Sulfinimines.

✍ Robert Kawecki 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Lewis Base Activation of Lewis Acids. Ad

Lewis Base Activation of Lewis Acids. Addition of Silyl Ketene Acetals to Aldehydes.

✍ Scott E. Denmark; Thomas Wynn; Gregory L. Beutner 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 233 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Lewis Base Activation of Lewis Acids. Ad

Lewis Base Activation of Lewis Acids. Addition of Silyl Ketene Acetals to Aldehydes

✍ Denmark, Scott E.; Wynn, Thomas; Beutner, Gregory L. 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 57 KB

Lewis Base Activation of Lewis Acids: Ca

Lewis Base Activation of Lewis Acids: Catalytic, Enantioselective Addition of Silyl Ketene Acetals to Aldehydes.

✍ Scott E. Denmark; Gregory L. Beutner; Thomas Wynn; Martin D. Eastgate 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 48 KB 👁 1 views

Lewis Base Activation of Lewis Acids: Ca

Lewis Base Activation of Lewis Acids: Catalytic, Enantioselective Addition of Silyl Ketene Acetals to Aldehydes

✍ Denmark, Scott E.; Beutner, Gregory L.; Wynn, Thomas; Eastgate, Martin D. 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 297 KB

High diastereoselectivity in lewis acid

High diastereoselectivity in lewis acid mediated aldol condensations using thioester silyl ketene acetals.

✍ Cesare Gennari; Anna Bernardi; Silvia Cardani; Carlo Scolastico 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 248 KB

BF30Et2 mediated aldol condensations of thioester silyl ketene acetals are stereoconvergent, and exhibit high internal (anti) and relative (Cram) diastereoselectivity.