Asymmetric selenocyclization with the use of dialkyl monoterpene diselenides

Tetrahedron Asymmetry

Volumn 19, Issue 2, 2008, Pages 223-230

  Rafiński, Zbigniew ^a   Ścianowski, Jacek ^a   Wojtczak, Andrzej ^a  

^a NICOLAUS COPERNICUS UNIVERSITY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALCOHOL DERIVATIVE; ALKYL GROUP; SELENIDE; TERPENE;

ARTICLE; ASYMMETRIC SYNTHESIS; CYCLIZATION; ENANTIOMER; PRIORITY JOURNAL;

EID: 38749094438     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.11.032     Document Type: Article

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14. 14 x = 0.14(5). Non-hydrogen atoms were refined anisotropically, hydrogen atoms were constrained as riding atoms. The (R, S, S, R)-C2, C1′, C2′ and C5′ chirality was determined. The structural data for 9 have been deposited at the Cambridge Crystallographic Data Centre: (CCDC No. 623526).
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