Nitro compounds
Patrick D. Bailey, Keith M. Morgan
Abstract
Patrick D. Bailey, Keith M. Morgan
Abstract
This chapter focuses on nitroso compounds. It refers to nitroso compounds as tautomeric with oximes that are thermodynamically more stable. The chapter shares diagrams to reference the bonding. C-nitroso compounds are readily turned to the corresponding oxime if there is a hydrogen-? linked to the nitroso group. Additionally, the chapter discusses the synthesis of aliphatic C-nitroso compounds, aromatic C-nitroso compounds, α-diketones via nitrosis compounds, N-nitroso compounds, and O-nitroso compounds. It mentions how aliphatic C-nitroso compounds tautomerizse to the oxime if an α-hydrogen is present. The α-chloro and acyl Cnitroso compounds are useful in terms of achieving the Diels-Alder reaction.
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This chapter focuses on nitroso compounds. It refers to nitroso compounds as tautomeric with oximes that are thermodynamically more stable. The chapter shares diagrams to reference the bonding. C-nitroso compounds are readily turned to the corresponding oxime if there is a hydrogen-? linked to the nitroso group. Additionally, the chapter discusses the synthesis of aliphatic C-nitroso compounds, aromatic C-nitroso compounds, α-diketones via nitrosis compounds, N-nitroso compounds, and O-nitroso compounds. It mentions how aliphatic C-nitroso compounds tautomerizse to the oxime if an α-hydrogen is present. The α-chloro and acyl Cnitroso compounds are useful in terms of achieving the Diels-Alder reaction.
Key concepts: Nitroso Compounds, Nitroso, Oxime, Chemistry, Tautomer, Nitro, Organic chemistry, Medicinal chemistry