A CONVENIENT ROUTE TO CARBOCYCLIC ANALOGS OF NUCLEOSIDES: (+/-) ARISTEROMYCIN

DOI: 10.1016/S0040-4039(00)71394-3

Source and publish data:

Tetrahedron Letters p. 133 - 136 (1980)

Update date:2022-07-30

Topics:: Authors:

Saksena, Anil K.

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Article abstract of DOI:10.1016/S0040-4039(00)71394-3

Stereocontrolled elaboration of cyclopentadien-azomethine adducts 1 and 2 led to a short total synthesis of (+/-) aristeromycin.In the course of this work a novel zinc reduction was observed.Also, ozonolysis of the gem-dihalo olefin 10 in metha

Full text of DOI:10.1016/S0040-4039(00)71394-3

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Article Doi

A CONVENIENT ROUTE TO CARBOCYCLIC ANALOGS OF NUCLEOSIDES: (+/-) ARISTEROMYCIN

DOI: 10.1016/S0040-4039(00)71394-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)71394-3

Full text of DOI:10.1016/S0040-4039(00)71394-3

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