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Thromboxane synthesis from glucose

Corey, E J, Shibasaki, M, Simple, J K, Stereocontrolled synthesis of thromboxane B2 from D-glucose, Tetrahedron Lett., 18, 1625-1626, 1977. [Pg.283]

Hanessian, S, LaveUee, P, Total synthesis of (4-)-thromboxane B2 from D-glucose. A detailed account. Can. J. Chem., 59, SlOSll, 1981. [Pg.283]

Corey, E. J., M. Shibasaki, and J. Knolle Simple Stereocontrolled Synthesis of Thromboxane B2 from Z)-Glucose. Tetrahedron Letters 1977, 1625. [Pg.56]

Reaction with aliyiic aicohois (1, 271-272 4, 167,5, 226-227). A key step in a recent, stereocontrolled synthesis of natural thromboxane Ba (4) from u-glucose... [Pg.399]

Carbohydrates have again been used as chiral precursors for the total synthesis of other natural products, including thromboxane Bj, ( —)-isoavenaciolide, and insect pheromones - but pride of place must be given to a total synthesis of (-l-)-biotin from o-glucose in which a biomimetic transformation was used in forming the tetrahydrothiophen ring (Chapter 23). [Pg.4]

Methyl 2,4-dideoxy-4-C-carboxymethyl-a-D-riZ o-hexopyranoside 2 -> 3 lactone (43), required as a key intermediate for the synthesis of optically active thromboxanes, has been synthesized from D-glucose by standard transformations. ... [Pg.120]

The au rie2Si group is used to protect in the synthesis of morphine, methynoLide from D-glucose, C+)-Aplasmomycin, thromboxane B and lOa-homothrom-boxane A, prostaglandin t d in carbapenein synthesis.3u Ph,Si protects OH in the preparation of the optically pure TriF fragment of acyl tetronic acid... [Pg.112]


See other pages where Thromboxane synthesis from glucose is mentioned: [Pg.171]    [Pg.206]    [Pg.167]    [Pg.320]    [Pg.1479]    [Pg.602]    [Pg.112]    [Pg.509]    [Pg.719]    [Pg.495]   
See also in sourсe #XX -- [ Pg.3 , Pg.226 , Pg.227 ]




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Thromboxanes

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