Literature DB >> 12713286

Systematic synthesis of Bis-THF ring cores in annonaceous acetogenins.

Naoyoshi Maezaki1, Naoto Kojima, Hiroaki Tominaga, Minori Yanai, Tetsuaki Tanaka.   

Abstract

Systematic synthesis of bis-THF ring cores, synthetic intermediates of adjacent bis-THF annonaceous acetogenins, has been achieved by asymmetric alkynylation and subsequent stereodivergent THF ring formation. The asymmetric alkynylation of alpha-tetrahydrofuranic aldehyde with (S)-3-butyne-1,2-diol derivatives gave good yields of erythro- and threo-adducts with very high diastereoselectivity. These adducts were converted into four types of bis-THF cores via two kinds of one-pot THF ring formation. [reaction: see text]

Entities:  

Year:  2003        PMID: 12713286     DOI: 10.1021/ol034131r

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


  3 in total

1.  Structure-antitumor activity relationship of hybrid acetogenins focusing on connecting groups between heterocycles and the linker moiety.

Authors:  Kaito Ohta; Tetsuya Fushimi; Mutsumi Okamura; Akinobu Akatsuka; Shingo Dan; Hiroki Iwasaki; Masayuki Yamashita; Naoto Kojima
Journal:  RSC Adv       Date:  2022-05-25       Impact factor: 4.036

2.  Palladium(0)-catalyzed synthesis of chiral ene-allenes using alkenyl trifluoroborates.

Authors:  Gary A Molander; Erin M Sommers; Sharon R Baker
Journal:  J Org Chem       Date:  2006-02-17       Impact factor: 4.354

Review 3.  Medicinal chemistry of Annonaceous acetogenins: design, synthesis, and biological evaluation of novel analogues.

Authors:  Naoto Kojima; Tetsuaki Tanaka
Journal:  Molecules       Date:  2009-09-17       Impact factor: 4.411

  3 in total

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