Circular dichroism, optical rotatory dispersion and absolute configuration of flavanones, 3-hydroxyflavanones and their glycosides

Volume: 26, Issue: 17, Pages: 4093 - 4108
Published: Jan 1, 1970
Abstract
Flavanones of 2S configuration and 3-hydroxyflavanones of 2R,3R configuration, having equatorial 2-aryl substituents in the former or diequatorial 2,3-substituents in the latter, exhibit a positive Cotton effect due to the n → π* transition (∼ 330 nm) and a negative Cotton effect in the n α π* region (∼ 280–290 nm). Flavanone glycosides possessing chiral aglycones show Cotton effects quite similar to their optically active aglycones while...
Paper Details
Title
Circular dichroism, optical rotatory dispersion and absolute configuration of flavanones, 3-hydroxyflavanones and their glycosides
Published Date
Jan 1, 1970
Volume
26
Issue
17
Pages
4093 - 4108
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