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A Protecting-Group-Free Route to Chiral BINOL–Phosphoric Acids

✍ Scribed by Baojian Li; Pauline Chiu


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
429 KB
Volume
2011
Category
Article
ISSN
1434-193X

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✦ Synopsis


Abstract

A two‐step, protecting group‐free route for the synthesis of 3,3′‐disubstituted and 6,6′‐disubstituted chiral BINOL–phosphoric acids has been realized starting from commercially available brominated BINOLs. This synthesis relies on the direct Suzuki coupling of brominated BINOL phosphoric acids. This synthetic strategy is more efficient compared to previous circuitous strategies involving protections and deprotections, and the process is higher yielding relative to the alternative two‐step synthesis involving Suzuki coupling of the BINOL.


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✍ Teng-Fei Niu; Chun Cai; Lan Yi 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 German ⚖ 264 KB

## Abstract By a one‐pot tandem __Ugi__ multicomponent reaction (MCR)/click reaction sequence not requiring protecting groups, 1__H__‐1,2,3‐triazole‐modified __Ugi__‐reaction products **6a**–**6n** (__Scheme 1__ and __Table 2__), **7a**–**7b** (__Table 4__), and **8** (__Scheme 2__) were synthesize