Concise substrate-controlled asymmetric total syntheses of dioxabicyclic marine natural products with 2,10-dioxabicyclo-[7.3.0]dodecene and 2,9-dioxabicyclo[6.3.0]undecene skeletons

Journal of the American Chemical Society

Volumn 134, Issue 49, 2012, Pages 20178-20188

  Kim, Mi Jung ^a   Sohn, Te Ik ^a   Kim, Deukjoon ^a   Paton, Robert S ^b  

^a Seoul National University   (South Korea)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE STEREOCHEMISTRY; ASYMMETRIC TOTAL SYNTHESIS; CHEMOSELECTIVE; COMPUTATIONAL ANALYSIS; CONFORMATIONAL EFFECT; DIANIONS; DODECENE; ENOLATE ALKYLATION; ENOLATES; GENERAL APPROACH; GLYCIDOL; MARINE NATURAL PRODUCTS; NATURAL PRODUCTS; RING CONFORMATIONS; TETRA-HYDROFURAN;

AMIDES; CYANIDES; MUSCULOSKELETAL SYSTEM; OLEFINS; STEREOCHEMISTRY; STEREOSELECTIVITY;

ALKYLATION;

GLYCIDOL; ISOLAURALLENE; ITOMANALLENE A; LAURALLENE; NATURAL PRODUCT; NEOLAURALLENE; NITRILE; PANNOSALLENE; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; ASYMMETRIC TOTAL SYNTHESIS; CHELATION; CHEMICAL STRUCTURE; ENANTIOMER; STEREOCHEMISTRY; SYNTHESIS;

BICYCLO COMPOUNDS, HETEROCYCLIC; BIOLOGICAL AGENTS; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; QUANTUM THEORY;

EID: 84870862154     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja310249u     Document Type: Article

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