A convenient enantioselective synthesis of natural (1R,3S)-amidinomycin

DOI: 10.1016/S0957-4166(97)00342-X

Source and publish data:

Tetrahedron Asymmetry p. 2679 - 2681 (1997)

Update date:2022-07-30

Topics:

Authors:

Nagata, Hiroshi

Taniguchi, Takahiko

Ogasawara, Kunio

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Article abstract of DOI:10.1016/S0957-4166(97)00342-X

Natural (1R,3S)-amidinomycin, an antiviral metabolite isolated from Streptomyces species, has been synthesized conveniently from (+)-norcamphor in an enantioselective manner.

Full text of DOI:10.1016/S0957-4166(97)00342-X

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Product name:((1S,3R)-3-[1,3]Dithian-2-yl-cyclopentyl)-carbamic acid benzyl ester

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