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Stereoselective Synthesis of the Pheromones of Ant Tetramorium Impurm and Leptogenys Diminuta
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作者 LI Yan HUANG Jin-xia +2 位作者 ZHOU Zhong-qiang CHEN Zu-xing XU Zhang-huang 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1999年第3期238-242,共5页
( 3R,4S )-4-Methyl-3-hexanol and ( 3R,4S )-4-methyl-3-heptanol, which are the pheromones of ant Tetramorium impurm and Leptogenys diminuta , were stereoselectively synthesized by six step sequence starting from N born... ( 3R,4S )-4-Methyl-3-hexanol and ( 3R,4S )-4-methyl-3-heptanol, which are the pheromones of ant Tetramorium impurm and Leptogenys diminuta , were stereoselectively synthesized by six step sequence starting from N bornane 10,2 sultam separately, the two asymmetric carbon atoms of the target products were created by employing asymmetric syn aldolization of N acylbornane 10,2 sultam with propylaldehyde. The enantiomeric excess of the target products prepared by this route is over 92%. 展开更多
关键词 PHEROMONE Asymmetric syn-aldolization N-Bornane-10 2 sultam
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