Pheromone synthesis, CVI. Synthesis of all of the four stereoisomers of tetrahydro‐2,2,6‐trimethyl‐2H‐pyran‐3‐ol, a volatile compound from the elm bark beetle Pteleobius vittatus
- 16 February 1988
- journal article
- notiz
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1988 (2) , 175-177
- https://doi.org/10.1002/jlac.198819880212
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Pheromone synthesis, CV. Synthesis of lactone components of the pheromone of Anastrepha suspensa, suspensolide, and the enantiomers of anastrephin and epianastrephinEuropean Journal of Organic Chemistry, 1988
- Pheromone Synthesis, XCVIII. Conversion of the Enantiomers of Sulcatol (6‐Methyl‐5‐hepten‐2‐ol) to the Enantiomers of Pityol [trans‐2‐(1‐Hydroxy‐1‐methylethyl)‐5‐methyltetrahydrofuran], a Male‐Specific Attractant of the Bark Beetle Pityophthorus pityographusEuropean Journal of Organic Chemistry, 1987
- Total synthesis of (±) BaiyunolTetrahedron Letters, 1986
- Solvomercuration-demercuration. 8. Oxymercuration-demercuration of methoxy-, hydroxy-. and acetoxy-substituted alkenesThe Journal of Organic Chemistry, 1981
- Reactions of alkylmercuric halides with sodium borohydride in the presence of molecular oxygenJournal of the American Chemical Society, 1974
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973
- Solvomercuration-demercuration. I. Oxymercuration-demercuration of representative olefins in an aqueous system. Mild procedure for the Markovnikov hydration of the carbon-carbon double bondThe Journal of Organic Chemistry, 1970