Enantioselective synthesis of the C3-C11 hydrocarbon fragment of the ionophore antibiotic tetronasin (ICI 139603)

DOI: 10.1016/S0040-4039(00)97888-2

Source and publish data:

Tetrahedron Letters p. 5521 - 5524 (1990)

Update date:2022-08-03

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Authors:

Ley Ley

Maw Maw

Trudell Trudell

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Article abstract of DOI:10.1016/S0040-4039(00)97888-2

The enantioselective synthesis of the C3-C11 fragment (2) of the novel ionophore tetronasin (1) has been completed via an intermediate enamine-enal-cyclisation of the dialdehyde (8) when treated with morpholine. The high degree of stereocontrol and asymme

Full text of DOI:10.1016/S0040-4039(00)97888-2

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