Stereoselective synthesis of highly substituted 8-oxabicyclo[3.2.1]octanes and 2,7-dioxatricyclo[4.2.1.0 3,8]nonanes

Tetrahedron

Volumn 68, Issue 29, 2012, Pages 5785-5792

  Khlevin, Dmitry A ^a   Sosonyuk, Sergey E ^a   Proskurnina, Marina V ^a   Zefirov, Nikolay S ^a,b  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b INSTITUTE OF PHYSIOLOGICALLY ACTIVE COMPOUNDS   (Russian Federation)

Author keywords

2,7 Dioxatricyclo 4.2.1.0 3,8 nonanes; 8 Oxabicyclo 3.2.1 octanes; Diastereoselectivity; Hydride reduction; Transannular hydroxycyclization

Indexed keywords

2,7 DIOXATRICYCLO[4.2.1.0]NONANE DERIVATIVE; 8 OXABICYCLO[3.2.1]OCTANE DERIVATIVE; ACETIC ACID DERIVATIVE; ALKENE; ANTINEOPLASTIC AGENT; BICYCLO[3.2.1]OCTANE DERIVATIVE; CARBASUGAR; CARBONYL DERIVATIVE; CYCLOHEPTANE DERIVATIVE; FURAN; GLYCOSIDASE INHIBITOR; HETEROCYCLIC COMPOUND; HYDROXYL GROUP; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; CRYSTAL STRUCTURE; CYCLIZATION; DRUG SYNTHESIS; ENZYME INHIBITION; HYDROXYLATION; NUCLEAR OVERHAUSER EFFECT; OXIDATION; POLYMERIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEREOCHEMISTRY; X RAY DIFFRACTION;

EID: 84862014283     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.05.029     Document Type: Article

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