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| 003 | MX-MdCICY | ||
| 005 | 20250625162442.0 | ||
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| 090 | _aB-20081 | ||
| 245 | 1 | 0 | _aPheromone Synthesis, CXLV. Synthesis of the Enantiomers of Rhynchophorol [(E)-6-Methyl-2-hepten-4-ol], the Male-Produced Aggregation Pheromone of the American Palm Weevil, Rhynchophorus palmarum |
| 490 | 0 | _vLiebigs Annalen der Chemie, 1992(11), p.1195-1198, 1992 | |
| 520 | 3 | _aBoth the enantiomers of rhynchophorol [(E)-6-methyl-2-hepten-4-ol (1)], the male-produced aggregation pheromone of the American palm weevil (Rhynchophorus palmarum), have been synthesized by reducing their precursors, (R)- and (S)-6-methyl-2-heptyn-4-ol (2), which have been prepared by lipasemediated asymmetric hydrolysis of the corresponding acetate and propionate. | |
| 650 | 1 | 4 | _aAMERICAN PALM WEEVIL |
| 650 | 1 | 4 | _aLIPASES |
| 650 | 1 | 4 | _aPHEROMONES |
| 650 | 1 | 4 | _aRHYNCHOPHOROL |
| 650 | 1 | 4 | _aRHYNCHOPHORUS PALMARUM |
| 650 | 1 | 4 | _aENZYMES |
| 700 | 1 | 2 | _aMori, K. |
| 700 | 1 | 2 | _aIshigami, K. |
| 856 | 4 | 0 |
_uhttps://drive.google.com/file/d/1x6Bmf3x3UWoZ7BDUCqEXzJNcI45yY5Wa/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
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