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.
📜 SIMILAR VOLUMES
## 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