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Org Lett ; 21(3): 758-761, 2019 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-30632762

RESUMO

The C3-C21 segment of aflastatin A has been synthesized by converging three segments including the C3-C8 segment, the C9-C15 segment, and the C16-C21 segment. Each segment has been synthesized from a vinylketene silyl N,O-acetal possessing a chiral auxiliary by a wide-range stereocontrol strategy. The C3-C8 segment was constructed in seven steps including the stereoselective vinylogous Mukaiyama alkylation, while the C9-C15 segment and the C16-C21 segment were synthesized using the vinylogous Mukaiyama aldol reaction in seven and eight steps, respectively.


Assuntos
Cetonas , Pirrolidinonas , Técnicas de Química Sintética , Etilenos/química , Cetonas/química , Pirrolidinonas/síntese química , Pirrolidinonas/química , Estereoisomerismo
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