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Optically active α-aminoalkylphosphonic acids 1 are structural analogues of α-amino acids
2, obtained by isosteric substitution of the planar and less bulky carboxylic acid (CO 2 H) by …

An efficient and versatile one-pot synthesis of 3, 6a-epoxyisoindoles annelated with oxazine,
oxazole, thiazine, thiazole, pyrimidine fragments and with their benzoannelated analogues …

Certain aromatic heterocycles are known to undergo Diels–Alder cycloaddition reactions
despite their aromaticity and hence expected decreased reactivity. In particular, the furanyl …

Organophosphorus Chemistry provides a comprehensive and critical review of the recent
literature. Coverage includes phosphines and their chalcogenides, phosphonium salts, low …

This review describes a comprehensive account of methods which are commonly applied for
the synthesis of α-heterocyclic/heteroaryl α-aminophosphonic acids and their esters. In the …

A novel and efficient nickel-catalyzed tandem 1, 4-1, 2-addition of P (O) H compounds to 1,
10-phenanthrolines forming various 2, 4-diphosphono-1, 2, 3, 4-tetrahydro-1, 10 …

The Diels–Alder reaction between 2, 5-dimethylfuran and vinylene carbonate was studied,
both from an experimental and a theoretical point of view. The system was shown to slowly …

Phosphonylated azaheterocycles are an important class of compounds with high biological
potential as conformationally restricted bioisosteres of amino acids. Therefore, it is of interest …

Well‐known and extensively studied for many decades, the Diels‐Alder reaction remains as
one of the most frequently employed synthetic methods for the construction of six‐membered …