Literature DB >> 23885858

Synthesis of high-value 1,6-enynes by tandem fragmentation/olefination.

Tung T Hoang1, Gregory B Dudley.   

Abstract

A tandem process provides high-value 1,6-enynes that are otherwise difficult to prepare. Two base-mediated reactions-fragmentation and olefination-are executed in a coordinated manner that is overall more efficient than either reaction on its own. The 1,6-enynes can be strategically employed in conjunction with carbocyclization to deliver important targets, as noted for reported syntheses of hirsutene and illudol.

Entities:  

Year:  2013        PMID: 23885858     DOI: 10.1021/ol401839e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Synthesis of "neoprofen", a rigidified analogue of ibuprofen, exemplifying synthetic methodology for altering the 3-D topology of pharmaceutical substances.

Authors:  Ron R Ramsubhag; Chelsea L Massaro; Christina M Dadich; Andrew J Janeczek; Tung T Hoang; Elizabeth A Mazzio; Suresh Eyunni; Karam F A Soliman; Gregory B Dudley
Journal:  Org Biomol Chem       Date:  2016-08-16       Impact factor: 3.876

2.  Synthesis, Molecular Pharmacology, and Structure-Activity Relationships of 3-(Indanoyl)indoles as Selective Cannabinoid Type 2 Receptor Antagonists.

Authors:  Harvey F Fulo; Amal Shoeib; Christian V Cabanlong; Alexander H Williams; Chang-Guo Zhan; Paul L Prather; Gregory B Dudley
Journal:  J Med Chem       Date:  2021-04-23       Impact factor: 7.446

  2 in total

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