Polycyclic trans-Fused Crown Ethers From D-Mannitol

DOI: 10.1016/S0040-4039(00)91776-3

Source and publish data:

Tetrahedron Letters p. 1287 - 1290 (1993)

Update date:2022-08-02

Topics:

Authors:

Nazhaoui, Mostafa

Gross, Bernard

Joly, Jean-Pierre

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Article abstract of DOI:10.1016/S0040-4039(00)91776-3

New macrocyclic ethers, all bearing a common trans-fused chiral dioxepan moiety, were easily synthesized from 1,3:4,6-di-O-benzylidene-D-mannitol in 5 or 6 steps (3 examples).The influence of the substituent at C-1/C-6 position upon conformation is discus

Full text of DOI:10.1016/S0040-4039(00)91776-3

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Product name:3,4-di-O-benzoyl-1,6-dibromo-1,6-dideoxy-2,5-O-methylene-D-mannitol

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