𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Diastereoselective schenck ene reaction of singlet oxygen with chiral allylic alcohols; access to enantiomerically enriched 1,2,4-trioxanes

✍ Scribed by Sunil Sabbani; Louise La Pensée; John Bacsa; Erik Hedenström; Paul M. O'Neill

Book ID
108283088
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
450 KB
Volume
65
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Singlet Oxygen Addition to Chiral Allyli
Singlet Oxygen Addition to Chiral Allylic Alcohols and Subsequent Peroxyacetalization with β-Naphthaldehyde: Synthesis of Diastereomerically Pure 3-β-Naphthyl-Substituted 1,2,4-Trioxanes.
✍ Axel G. Griesbeck; Tamer T. El-Idreesy; Johann Lex 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 41 KB

## 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.

ChemInform Abstract: Regio- and Diastere
ChemInform Abstract: Regio- and Diastereoselective Ene Reaction of 4-Phenyl-1,2,4-triazoline-3,5-dione with Chiral Allylic Alcohols and Their Derivatives.
✍ Ay-Hua Gau; Guey-Liang Lin; Biing-Jiun Uang; Fen-Ling Liao; Sue-Lein Wang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Regio-and Diastereoselective Ene Reaction of 4-Phenyl-1,2,4triazoline-3,5-dione with Chiral Allylic Alcohols and Their Derivatives. -Allylic alcohols and their methyl ethers and acetates react with triazolinedione (II) with complete regioselectivity and, in most cases, with high diastereoselectivit