A simple enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecane via intramolecular asymmetric oxyselenenylation: A new route to optically active spiroketals

Tetrahedron Letters

Volumn 42, Issue 10, 2001, Pages 1931-1934

  Uchiyama, Masahiko ^a   Oka, Masako ^a   Harai, Satohide ^a   Ohta, Akihiro ^a  

^a TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

Author keywords

1,7 dioxaspiro 5.5 undecane; Chiral diselenide; Enantioselective synthesis; Insect pheromone; Intramolecular asymmetric oxyselenenylation; Spiroketal

Indexed keywords

1,7 DIOXASPIRO[5.5]UNDECANE; 4 (3,4 DIHYDRO 2H PYRAN 6 YL)BUTAN 1 OL; ACETAL DERIVATIVE; PHEROMONE; PYRAN DERIVATIVE; SPIROKETAL; UNCLASSIFIED DRUG;

ARTICLE; DROSOPHILA; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY; TEMPERATURE;

BACTROCERA OLEAE; DROSOPHILA MELANOGASTER; INSECTA;

EID: 0035804472     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)00024-7     Document Type: Article

References (31)