Total synthesis of sandresolide B and amphilectolide

Ingrid T. Chen; Irina Baitinger; Lucas Schreyer; Dirk Trauner

doi:10.1021/ol403156r

Total synthesis of sandresolide B and amphilectolide

Ingrid T. Chen, Irina Baitinger, Lucas Schreyer, Dirk Trauner

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

The total synthesis of the diterpenoids sandresolide B and amphilectolide from a common furan building block is presented. Key steps include palladium-mediated carbonylation, lanthanide catalyzed ring closure, Myers alkylation, intramolecular Friedel-Crafts acylation, photooxygenation, and a Kornblum-DeLaMare rearrangement.

Original language	English (US)
Pages (from-to)	166-169
Number of pages	4
Journal	Organic Letters
Volume	16
Issue number	1
DOIs	https://doi.org/10.1021/ol403156r
State	Published - Jan 3 2014

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol403156r

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title = "Total synthesis of sandresolide B and amphilectolide",

abstract = "The total synthesis of the diterpenoids sandresolide B and amphilectolide from a common furan building block is presented. Key steps include palladium-mediated carbonylation, lanthanide catalyzed ring closure, Myers alkylation, intramolecular Friedel-Crafts acylation, photooxygenation, and a Kornblum-DeLaMare rearrangement.",

author = "Chen, {Ingrid T.} and Irina Baitinger and Lucas Schreyer and Dirk Trauner",

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Total synthesis of sandresolide B and amphilectolide

Abstract

ASJC Scopus subject areas

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