Highly trans-Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ-Deoxygenation and Heck-Matsuda Reaction: Asymmetric Total Synthesis of (-)-Musellarins A-C and Their Analogues

Chemistry - A European Journal

Volumn 21, Issue 31, 2015, Pages 11152-11157

  Li, Zhilong ^a   Ip, Fanny C F ^a   Ip, Nancy Y ^a   Tong, Rongbiao ^a  

^a HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

Author keywords

Achmatowicz rearrangement; arylation; musellarins; total synthesis; zinc

Indexed keywords

STEREOSELECTIVITY; SYNTHESIS (CHEMICAL); ZINC;

ACHMATOWICZ REARRANGEMENT; ARYLATION REACTIONS; ARYLATIONS; ASYMMETRIC TOTAL SYNTHESIS; EFFICIENT SYNTHESIS; HECK-MATSUDA REACTIONS; MUSELLARINS; TOTAL SYNTHESIS; DIASTEREOSELECTIVE;

AROMATIC COMPOUNDS;

3,4-DIHYDROPYRAN; HEPTANE DERIVATIVE; MUSELLARIN A; MUSELLARIN B; MUSELLARIN C; PYRAN DERIVATIVE; ZINC;

CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

DIARYLHEPTANOIDS; OXIDATION-REDUCTION; PYRANS; STEREOISOMERISM; ZINC;

EID: 84945980847     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201501713     Document Type: Article

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