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Synthesis and absolute configuration of optically active selenoxides. X-Ray molecular structure of (–) se-4-menthyloxycarbonylphenyl 2, 4, 6-tri-isopropylphenyl selenoxide
Microbial metabolites. Part XI. Total synthesis and absolute configuration of (S)-carlosic acid (4-butyryl-2, 5-dihydro-3-hydroxy-5-oxo-furan-2-acetic acid) and conversion of (R)-5-methyltetronic acid into (R)-carolic acid {3, 4-dihydro-8-methylfuro [3, 4-b] oxepin-5, 6 (2 H, 8 H)-di-one}
Quantitative studies in stereochemistry. 16. The ratio of diastereomeric pinacols produced in the aluminum amalgam bimolecular reduction of acetophenone
NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 30. RING ENLARGEMENT OF CYCLOALKANONES WITH BENZYLSULFONYLDIAZOMETHANE AND CONVERSION OF THE RESULTING HOMOLOGATED 2-BENZYLSULFONYLCYCLOALKANONES TO 1-BENZYLSULFONYL-1-CYCLOALKENES VIA CHELETROPIC RING CONTRACTION