Literature DB >> 17020310

Application of the B-alkyl suzuki-miyaura cross-coupling reaction to the stereoselective synthesis of analogues of (3S)-oxidosqualene.

Johan M Winne1, Bing Guang, Jo D'Herde, Pierre J De Clercq.   

Abstract

[reaction: see text] A general method is described for the direct and stereoselective synthesis of epoxypolyenes via Suzuki-Miyaura cross-coupling reaction of 1-iodoalkenes with B-alkylboron compounds. It allows for the straightforward and convergent assembly of compounds that are structurally similar to (3S)-oxidosqualene, an important intermediate in steroid biosynthesis.

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Year:  2006        PMID: 17020310     DOI: 10.1021/ol061962z

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis of cananodine by intramolecular epoxide opening.

Authors:  Patrick Shelton; Toby J Ligon; Jennifer M Dell Née Meyer; Loagan Yarbrough; James R Vyvyan
Journal:  Tetrahedron Lett       Date:  2017-07-25       Impact factor: 2.415

2.  Cyclohexanecarbonitriles: assigning configurations at quaternary centers from (13)C NMR CN chemical shifts.

Authors:  Fraser F Fleming; Guoqing Wei
Journal:  J Org Chem       Date:  2009-05-01       Impact factor: 4.354

Review 3.  Catalytic enantioselective synthesis of chiral organic compounds of ultra-high purity of >99% ee.

Authors:  Ei-ichi Negishi; Shiqing Xu
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2015       Impact factor: 3.493

  3 in total

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