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STEPWISE PHOSPHORYLATION OF VICINAL DIOL AND STERICALLY HINDERED ALCOHOL DIRECTED TOWARD D-MYO-INOSITOL 2,4,5-TRISPHOSPHATE

DOI: 10.1016/S0040-4039(00)96160-4

Source and publish data:

Tetrahedron Letters p. 2607 - 2610 (1987)

Update date:2022-08-03

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Authors:

Watanabe, YutakaWatanabe, Yutaka

Ogasawara, TomioOgasawara, Tomio

Shiotani, NaokazuShiotani, Naokazu

Ozaki, ShoichiroOzaki, Shoichiro

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Article abstract of DOI:10.1016/S0040-4039(00)96160-4

Synthesis of l-menthoxyacetic esters of properly protected DL-myo-inositol 2,4,5-trisphosphate was accomplished.This process involves stepwise phosphorylation of sterically hindered and vicinally situated alcohols according to the procedure treating succe

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Full text of DOI:10.1016/S0040-4039(00)96160-4

Products guided by the article

Product name:((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-acetic acid (1S,2R,3S,4S,5R,6R)-2,5-bis-benzyloxy-6-(bis-benzyloxy-phosphoryloxy)-3,4-bis-(4-methoxy-benzyloxy)-cyclohexyl ester

Cas No:111408-71-0

111408-71-0

R&D Labs maybe for 111408-71-0

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