✦ LIBER ✦

A new strategy for the synthesis of unsymmetrical phosphotriesters

✍ Scribed by Hu Jun; Ding Yi-Xiang

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 256 KB
Volume: 18
Category: Article
ISSN: 0256-7660
DOI: 10.1002/cjoc.20000180218

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Strategy for the Stereoselective Synth

A Strategy for the Stereoselective Synthesis of Unsymmetric Atropisomeric Ligands: Preparation of NAPhePHOS, a New Biaryl Diphosphine

✍ Guillaume Michaud; Michel Bulliard; Louis Ricard; Jean-Pierre Genêt; Angela Mari 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 104 KB 👁 2 views

A Strategy for the Stereoselective Synth

A Strategy for the Stereoselective Synthesis of Unsymmetric Atropisomeric Ligands: Preparation of NAPhePHOS, a New Biaryl Diphosphine.

✍ Guillaume Michaud; Michel Bulliard; Louis Ricard; Jean-Pierre Genet; Angela Mari 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

A New, Iterative Strategy for the Synthe

A New, Iterative Strategy for the Synthesis of Unsymmetrical Polyynes: Application to the Total Synthesis of 15,16-Dihydrominquartynoic Acid.

✍ Sanghee Kim; Shinae Kim; Taeho Lee; Hyojin Ko; Deukjoon Kim 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 160 KB 👁 1 views

A New Strategy for the Diastereoselectiv

A New Strategy for the Diastereoselective Synthesis of Polyfunctionalized Pyrrolidines.

✍ Andrew S. Davis; Nicole J. Gates; Karl B. Lindsay; Minyan Tang; Stephen G. Pyne 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 118 KB 👁 2 views

New Strategy for the Synthesis of Tetrah

New Strategy for the Synthesis of Tetrahydroisoquinoline Alkaloids.

✍ Philip Magnus; Kenneth S. Matthews; Vince Lynch 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 213 KB 👁 2 views

A new synthesis of unsymmetrically subst

A new synthesis of unsymmetrically substituted halophosphines

✍ Jan Omelańczuk 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 261 KB

## Abstract Chiral, racemic alkylaryl‐, or diarylhalophosphines have been obtained in 50–70% yields by treatment of alkylaryl‐ or diaryl‐methylthiohalophosphonium triflates with triphenylphosphine in methylene chloride solution at room temperature or under reflux.