## Abstract The addition of hypophosphorous acid to an azomethine bond of __N__‐(__R__)‐α‐methylbenzyl Schiff bases of a variety of aldehydes led to the formation of __N__‐(__R__)‐α‐methylbenzylamino‐(__S__)‐methanephosphonous acids in 100% diastereoselectivity. This fact allows us to suggest the p
✦ LIBER ✦
ChemInform Abstract: Diastereoselective Addition of Hypophosphorous Acid to N-(R)-α-Methylbenzyl-Substituted Schiff Bases.
✍ Scribed by Jaroslaw Lewkowski; Rafal Karpowicz; Malgorzata Rybarczyk
- Publisher
- John Wiley and Sons
- Year
- 2008
- Weight
- 24 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Diastereoselective addition of hypophosp
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