4.6 Article

Catalytic asymmetric 1,2-Addition/Lactonization tandem reactions for the syntheses of chiral 3-Substituted phthalides using organozinc reagents

Journal

APPLIED ORGANOMETALLIC CHEMISTRY
Volume 33, Issue 1, Pages -

Publisher

WILEY
DOI: 10.1002/aoc.4643

Keywords

addition,catalysis, lactonization; phthalide; tandem reaction

Funding

  1. Nature Science Foundation of Fujian Province, China [2016J01086]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB20000000]
  3. Chinese Academic of Sciences
  4. Fujian Institute of Research on the Structure of Matter
  5. Key Laboratory of Coal to Ethylene Glycol and Its Related Technology
  6. Priority Research Program of the Chinese Academy of Sciences

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Using chiral phosphoramide ligand 2d-Zn (II) complex derived from (1R,2R)-1,2-diphenylethylenediamine as the catalyst, we have developed efficient catalytic asymmetric 1,2-addition/lactonization tandem reactions of diverse organozinc reagents with varied methyl 2-formylbenzoates for the construction of optically enriched 3-aryl or alkyl substituted phthalides, which are significant building blocks of many important chiral pharmaceuticals and natural products. The corresponding products could be afforded with good to excellent yields (up to 95%) and moderate to good enantioselectivities (up to 89%).

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