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Diverse reactivity of 2-formylphenylboronic acid with secondary amines: synthesis of 3-amino-substituted benzoxaboroles
✍ Scribed by Agnieszka Adamczyk-Woźniak; Izabela Madura; Aldrik H. Velders; Andrzej Sporzyński
- Book ID
- 104098369
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 380 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
a b s t r a c t
In the reaction of 2-formylphenylboronic acid with secondary amines different products are formed depending on the structure of the amines. For aliphatic amines the reaction proceeds with the formation of 3-amino-substituted benzoxaboroles or with the formation of complexed boroxins. A crystal structure of the benzoxaborole with a thiomorpholinyl substituent was determined.
📜 SIMILAR VOLUMES
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## Abstract The aminomethylation of the derivatives of trivalent organophosphorus acids, containing PH and POSiMe~3~ fragments with various bis‐ and tris(alkoxymethyl)amines and bis(alkoxymethyl)amino acids, is proposed as a convenient method for the synthesis of new bis‐ and trisphosphorylated ami