✦ LIBER ✦

Hydroboration/Intramolecular Reduction of Allyl Ketones with (Diisopinocampheyl)borane: A Convenient Synthesis of Enantiomerically Enriched 1,4-Diols

✍ Scribed by Molander, Gary A.; Bobbitt, Kevin L.

Book ID: 127348637
Publisher: American Chemical Society
Year: 1994
Tongue: English
Weight: 368 KB
Volume: 59
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00089a005

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Highly Diastereoselective TiCl4-Mediat

A Highly Diastereoselective TiCl4-Mediated Reduction of β-Hydroxy Ketones with BH3·py — A Very Efficient and General Synthesis of syn-1,3-Diols

✍ Giuseppe Bartoli; Marcella Bosco; Enrico Marcantoni; Massimo Massaccesi; Samuele 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 332 KB 👁 1 views

ChemInform Abstract: A Highly Diastereos

ChemInform Abstract: A Highly Diastereoselective TiCl4-Mediated Reduction of β-Hydroxy Ketones with BH3×Py — A Very Efficient and General Synthesis of syn-1,3-Diols.

✍ Giuseppe Bartoli; Marcella Bosco; Enrico Marcantoni; Massimo Massaccesi; Samuele 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 41 KB 👁 1 views