✦ LIBER ✦

ChemInform Abstract: The Use of Phosphinamide N-Protecting Groups in the Diastereoselective Reduction of Ketones.

✍ Scribed by M. J. PALMER; J. R. STUDLEY; T. C. WALSGROVE; M. WILLS

Publisher: John Wiley and Sons
Year: 2010
Weight: 39 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199844039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: The Use of Phosphin

ChemInform Abstract: The Use of Phosphinamide N-Protecting Groups in the Diastereoselective Reduction of Ketones

✍ M. J. PALMER; J. R. STUDLEY; T. C. WALSGROVE; M. WILLS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

Lewis Acid Mediated Diastereoselective R

Lewis Acid Mediated Diastereoselective Reduction of N-Protected β-Amino Ketones: Influence of the Nature of the Metal Atom and of the Nitrogen Protecting Group.

✍ Giuseppe Bartoli; Massimo Bartolacci; Manuela Cortese; Enrico Marcantoni; Massim 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 127 KB

ChemInform Abstract: A Novel Phosphinami

ChemInform Abstract: A Novel Phosphinamide Catalyst for the Asymmetric Reduction of Ketones by Borane.

✍ M. P. GAMBLE; A. R. C. SMITH; M. WILLS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

A Novel Phosphinamide Catalyst for the Asymmetric Reduction of Ketones by Borane. -The novel phosphinamide ("cat.") is a readily available, robust, versatile and recoverable reagent for the catalytic asymmetric reduction of ketones by borane. -(GAMBLE, M.

ChemInform Abstract: Highly Diastereosel

ChemInform Abstract: Highly Diastereoselective α-Mannopyranosylation in the Absence of Participating Protecting Groups.

✍ David Crich; Weiling Cai; Zongmin Dai 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB

ChemInform Abstract: Chiral Phosphinamid

ChemInform Abstract: Chiral Phosphinamides: New Catalysts for the Asymmetric Reduction of Ketones by Borane.

✍ B. BURNS; N. P. KING; H. TYE; J. R. STUDLEY; M. GAMBLE; M. WILLS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

The Use of Cyclic Bifunctional Protectin

The Use of Cyclic Bifunctional Protecting Groups in Oligosaccharide Synthesis

✍ Remy E. J. N. Litjens; Leendert J. Van den Bos; Jeroen D. C. Codee; Herman S. Ov 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 11 KB 👁 1 views