Reductions by hydrides and hydroboration. The stereoselectivity of new access methods to 3-arylmethyl-4-chromanones (homoisoflavone derivatives)

DOI: 10.1016/S0040-4020(01)89754-4

Source and publish data:

Tetrahedron p. 1849 - 1858 (1990)

Update date:2022-07-29

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Authors:

Gomis Gomis

Kirkiacharian

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Article abstract of DOI:10.1016/S0040-4020(01)89754-4

The reduction of 3-arylmethyl-4-chromanones by sodium borohydride, lithium tri-tert-butoxyaluminum hydride and hydroboration followed by oxydation of 3-benzyl-4-hydroxy-coumarines lead to mixtures of Cis and Trans diastereoisomers of 3-arylmethyl-4-chroma

Full text of DOI:10.1016/S0040-4020(01)89754-4

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