Harnessing the Intrinsic Reactivity within the Aplysinopsin Series for the Synthesis of Intricate Dimers: Natural from Start to Finish

Synthesis (Germany)

Volumn 47, Issue 16, 2015, Pages 2367-2376

  Skiredj, Adam ^a   Beniddir, Mehdi A ^a   Joseph, Delphine ^a   Bernadat, Guillaume ^b   Evanno, Laurent ^a   Poupon, Erwan ^a  

^a CNRS   (France)

^b UNIVERSITÉ PARIS SUD   (France)

Author keywords

alkaloids; aplysinopsins; biomimetic synthesis; natural products; total synthesis

Indexed keywords

ALKALOIDS; BIOMIMETICS; BIOSYNTHESIS; DIMERS; METABOLITES; MONOMERS; SYNTHESIS (CHEMICAL);

APLYSINOPSINS; BIOMIMETIC SYNTHESIS; BIOSYNTHETIC PRECURSORS; FUTURE PROSPECTS; INTRINSIC REACTIVITY; MARINE ALKALOIDS; NATURAL PRODUCTS; TOTAL SYNTHESIS;

BIOMIMETIC PROCESSES;

ALKALOID DERIVATIVE; APLYSINOPSIN DERIVATIVE; CHEMICAL COMPOUND; CYCLOAPLYSINOPSIN A; CYCLOAPLYSINOPSIN B; CYCLOBUTANE DERIVATIVE; DICTAZOLE B; DIMER; HYDANTOIN; MONOMER; PYRROLE DERIVATIVE; TUBASTRINDOLE B; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMPLEX FORMATION; DIMERIZATION; PRECURSOR; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 84938349199     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0034-1381032     Document Type: Article

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