PHEROMONE SYNTHESIS .88. SYNTHESIS OF ALL OF THE 4 POSSIBLE STEREOISOMERS OF 5-HYDROXY-4-METHYL-3-HEPTANONE (SITOPHILURE), THE AGGREGATION PHEROMONE OF THE RICE WEEVIL AND THE MAIZE WEEVIL

被引:43
作者
MORI, K
EBATA, T
机构
关键词
D O I
10.1016/S0040-4020(01)87281-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:4421 / 4426
页数:6
相关论文
共 13 条
[1]   PHEROMONE SYNTHESIS .44. STEREOSELECTIVE SYNTHESIS OF ERYTHRO-SERRICORNIN, (4R,6R,7S)-4,6-DIMETHYL-7-HYDROXYNONAN-3-ONE AND (4S,6R,7S)-4,6-DIMETHYL-7-HYDROXYNONAN-3-ONE, STEREOISOMERS OF THE SEX-PHEROMONE OF CIGARETTE BEETLE [J].
CHUMAN, T ;
KOHNO, M ;
KATO, K ;
NOGUCHI, M ;
NOMI, H ;
MORI, K .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1981, 45 (09) :2019-2023
[2]   NUCLEAR MAGNETIC-RESONANCE ENANTIOMER REAGENTS - CONFIGURATIONAL CORRELATIONS VIA NUCLEAR MAGNETIC-RESONANCE CHEMICAL-SHIFTS OF DIASTEREOMERIC MANDELATE, O-METHYLMANDELATE, AND ALPHA-METHOXY-ALPHA-TRIFLUOROMETHYLPHENYLACETATE (MTPA) ESTERS [J].
DALE, JA ;
MOSHER, HS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (02) :512-519
[3]   STEREOSPECIFIC SYNTHESIS OF (+)-(3R,4R)-4-METHYL-3-HEPTANOL - ENANTIOMER OF A PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE (SCOLYTUS-MULTISTRIATUS) [J].
FRATER, G .
HELVETICA CHIMICA ACTA, 1979, 62 (08) :2829-2832
[4]  
HASEGAWA J, 1981, J FERMENT TECHNOL, V59, P257
[5]   ACYCLIC STEREOSELECTION .4. ASSIGNMENT OF STEREOSTRUCTURE TO BETA-HYDROXYCARBONYL COMPOUNDS BY C-13 NUCLEAR MAGNETIC-RESONANCE [J].
HEATHCOCK, CH ;
PIRRUNG, MC ;
SOHN, JE .
JOURNAL OF ORGANIC CHEMISTRY, 1979, 44 (24) :4294-4299
[6]   PHEROMONE SYNTHESIS .80. SYNTHESIS OF (3R,4S)-4-METHYL-3 HEXANOL, THE PHEROMONE OF THE ANT TETRAMORIUM-IMPURUM [J].
KATO, M ;
MORI, K .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1985, 49 (10) :3073-3075
[7]   OXIDATION OF LONG-CHAIN AND RELATED ALCOHOLS TO CARBONYLS BY DIMETHYL-SULFOXIDE ACTIVATED BY OXALYL CHLORIDE [J].
MANCUSO, AJ ;
HUANG, SL ;
SWERN, D .
JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (12) :2480-2482
[8]   PHEROMONE SYNTHESIS .66. A NEW SYNTHESIS OF SERRICORNIN [(4S,6S,7S)-7-HYDROXY-4,6-DIMETHYL-3-NONANONE], THE SEX-PHEROMONE OF THE CIGARETTE BEETLE [J].
MORI, K ;
WATANABE, H .
TETRAHEDRON, 1985, 41 (16) :3423-3428
[10]   PREPARATIVE BIOORGANIC CHEMISTRY .6. BIOCHEMICAL PREPARATIONS OF BOTH THE ENANTIOMERS OF METHYL 3-HYDROXYPENTANOATE AND THEIR CONVERSION TO THE ENANTIOMERS OF 4-HEXANOLIDE, THE PHEROMONE OF TROGODERMA-GLABRUM [J].
MORI, K ;
MORI, H ;
SUGAI, T .
TETRAHEDRON, 1985, 41 (05) :919-925