| ID | 113450 |
| 著者 |
Kang, Bubwoong
Kyoto University
Wang, Yinli
Kyoto University
Kuwano, Satoru
Kyoto University
Yamaoka, Yousuke
Kyoto University
Takasu, Kiyosei
Kyoto University
|
| 資料タイプ |
学術雑誌論文
|
| 抄録 | A highly site-selective N-heterocyclic carbene (NHC)-catalyzed benzoin-type cyclization of unsymmetrical dialdoses is developed to enable a divergent cyclitol synthesis. The choice of chiral NHCs and protecting groups affects the site-selectivity. The resulting inososes are converted into epi-, muco- and myo-inositol, and their chiral protected derivatives are formed in good yields.
|
| 掲載誌名 |
Chemical Communications
|
| ISSN | 13597345
1364548X
|
| cat書誌ID | AA11071130
AA12455105
|
| 出版者 | The Royal Society of Chemistry
|
| 巻 | 53
|
| 号 | 32
|
| 開始ページ | 4469
|
| 終了ページ | 4472
|
| 発行日 | 2017-03-29
|
| 権利情報 | ©The Royal Society of Chemistry 2017
|
| EDB ID | |
| 出版社版DOI | |
| 出版社版URL | |
| フルテキストファイル | |
| 言語 |
eng
|
| 著者版フラグ |
著者版
|
| 部局 |
薬学系
|
