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Stereoselective synthesis of (+)-flutriafol
- Chang, Minsun;
- Kim, Tae Hyun;
- Kim, Hee-Doo
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WEB OF SCIENCE
17Citations
SCOPUS
16초록
The stereoselective synthesis of (+)-flutriafol, a triazole fungicide, has been accomplished in seven linear steps from (1S)-[(4R)-2,2-dimethyl-[1,3]-dioxotan-4-yl]-(4-methoxyphenyl)methanol in 15% overall yield. Diastereoselective nucleophilic 1,2-addition was employed as a key step for constructing the requisite chiral 1,2-diol for flutriafol. A high degree of 1,4-asymmetric induction could be realized via a chelation-controlled mechanism during the key alkylation step. (C) 2008 Elsevier Ltd. All rights reserved.
키워드
ASYMMETRIC NUCLEOPHILIC-ADDITION; ALKYLATION; FUNGICIDES; AUXILIARY; SILYLOXY; ETHER
- 제목
- Stereoselective synthesis of (+)-flutriafol
- 저자
- Chang, Minsun; Kim, Tae Hyun; Kim, Hee-Doo
- 발행일
- 2008-06-30
- 유형
- Article
- 권
- 19
- 호
- 12
- 페이지
- 1504 ~ 1508