THE OXIRANE RING OPENINGS OF THE DIANHYDRO SUGAR WITH HIGH REGIOSELETIVITY AND ITS USE IN PREPARATION OF TWO CHIRAL SEGMENTS OF 6-DEOXYERYTHRONOLIDE B

DOI: 10.1016/S0040-4039(00)85401-5

Source and publish data:

Tetrahedron Letters p. 6071 - 6074 (1986)

Update date:2022-08-03

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Authors:

Wakamatsu, Takeshi

Nakamura, Hideo

Nishimiki, Yuji

Yoshida, Kaoru

Noda, Tomoko

Taniguchi, Masato

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Article abstract of DOI:10.1016/S0040-4039(00)85401-5

The oxirane ring of the dianhydro sugar 2 obtained from levoglucosan (1,6-anhydro-β-D-glucose) is opened regioselectively with organometallic carbon nucleophiles and its application to an asymmetric synthesis of the C₁-C₅ segment 9 t

Full text of DOI:10.1016/S0040-4039(00)85401-5

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