@article{oai:toyama.repo.nii.ac.jp:00015771,
 author = {豊岡, 尚樹 and 神, 誠 and 西野, 彰 and 田中, 敬子 and 吉田, 泰子 and 百瀬, 雄章},
 journal = {天然有機化合物討論会講演要旨集, Symposium on the Chemistry of Natural Products, symposium papers},
 month = {Sep},
 note = {application/pdf, Biocatalysis is recognized as a useful tool for organic synthesis, especially for the asymmetric synthesis of natural products. As part of our efforts to synthesize versatile chiral building blocks by adopting biocatalysis, we developed the lipase-catalyzed desymmetrization of the meso-glycol 1 and the meso-diacetate 2 to afford both enantiomers of the ketol acetate 4 as an optically pure state, respectively. The desymmetrization of the meso-glycol 5 was also achieved to give the monoacetate (-)-6, which was led in three steps to the decalin (+)-19. Enantiomerization of (+)-19 was readily accomplished to give (-)-19. On the other hand, baker's yeast reduction of the β-keto ester 7 proceeded in a highly enantioselective manner and furnished the homochiral piperidone (-)-8 in good yield. The enantiomer (+)-8 was obtained by the lipase-mediated optical resolution of (±)-8. Thus, we achieved highly efficient synthesis of both enantiomers of chiral building blocks 4, 6, 8. The versatility of 4, 6 and 8 for natural product synthesis was demonstrated by the first total synthesis of(-)-cassine (11), (+)-spectaline (12), (-)-indolizidine 235B' and the formal synthesis of (-)-dihydropinidine, (-)-indolizidine 207A, 209B, (-)-polygodial, (-)-warburganal, (-)-drimenin, and prosopinie, respectively., Article, 天然有機化合物討論会講演要旨集 36, 234-241.(1994)},
 pages = {234--241},
 title = {31 生体触媒を活用した汎用性キラル素子の創製と天然物合成への応用(口頭発表の部)},
 volume = {36},
 year = {1994}
}