Literature DB >> 11412965

Synthesis and absolute configuration of Stellettadine A: a marine alkaloid that induces larval metamorphosis in ascidians.

D Nozawa1, H Takikawa, K Mori.   

Abstract

Stellettadine A, a bisguanidinium alkaloid isolated from a marine sponge Stelletta sp. as an inducer of larval metamorphosis in ascidians, and its unnatural enantiomer were synthesized from the enantiomers of citronellal. The absolute configuration of stellettadine A was established as R.

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Year:  2001        PMID: 11412965     DOI: 10.1016/s0960-894x(01)00015-4

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Progress toward the De Novo Asymmetric Synthesis of Euphanes.

Authors:  HtooTint Wai; Thomas Koelblen; Matthew E Hayes; Thomas P Burris; Glenn C Micalizio
Journal:  Org Lett       Date:  2022-05-18       Impact factor: 6.072

2.  Synthesis of (+/-)-bistellettadine A.

Authors:  Min Yu; Susan S Pochapsky; Barry B Snider
Journal:  Org Lett       Date:  2010-02-19       Impact factor: 6.005

  2 in total

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