| Literature DB >> 29893133 |
Bradley T Reid1, Artur K Mailyan1, Armen Zakarian1.
Abstract
Protecting-group-free total synthesis of (+)-guadinomic acid is reported using δ-valerolactone as a readily available starting material. The protocol utilizes the recent hydroxyl-directed guanidylation of unactivated alkenes as an approach for direct stereoselective incorporation of the guanidine unit furnishing the natural product in 7 steps.Entities:
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Year: 2018 PMID: 29893133 PMCID: PMC6309422 DOI: 10.1021/acs.joc.8b01214
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354