A synthetic route to highly substituted 1,2,3,4-tetrahydroisoquinolines via Yb(OTf)3-catalyzed diastereoselective ring opening of bridged oxazolidines: Asymmetric synthesis of 2-azapodophyllotoxin

Chemistry - A European Journal

Volumn 17, Issue 17, 2011, Pages 4905-4913

  Srivastava, Ajay Kumar ^a   Koh, Minseob ^a   Park, Seung Bum ^a  

^a Seoul National University   (South Korea)

Author keywords

2 azapodophyllotoxin; Garner aldehyde; natural products; tetrahydroisoquinoline; total synthesis

Indexed keywords

2-AZAPODOPHYLLOTOXIN; GARNER ALDEHYDE; NATURAL PRODUCTS; TETRAHYDROISOQUINOLINES; TOTAL SYNTHESIS;

AROMATIC COMPOUNDS; CATALYSIS; STEREOSELECTIVITY; YTTERBIUM;

ALDEHYDES;

1,2,3,4-TETRAHYDROISOQUINOLINE; 2 AZAPODOPHYLLOTOXIN; 2-AZAPODOPHYLLOTOXIN; BRIDGED COMPOUND; DRUG DERIVATIVE; LEWIS ACID; OXAZOLE DERIVATIVE; OXAZOLIDINE; PODOPHYLLOTOXIN; TETRAHYDROISOQUINOLINE; TETRAHYDROISOQUINOLINE DERIVATIVE; YTTERBIUM;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

BRIDGED COMPOUNDS; CATALYSIS; LEWIS ACIDS; MOLECULAR STRUCTURE; OXAZOLES; PODOPHYLLOTOXIN; STEREOISOMERISM; TETRAHYDROISOQUINOLINES; YTTERBIUM;

EID: 79953854409     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002938     Document Type: Article

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