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Volumn 79, Issue 18, 2014, Pages 8835-8849

Total synthesis of (-)-4-hydroxyzinowol

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; DRUG THERAPY; FUNCTIONAL GROUPS; GLYCOPROTEINS; MOLECULES; ORGANIC SOLVENTS;

EID: 84911873518     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo501666x     Document Type: Article
Times cited : (37)

References (85)
  • 83
    • 84911869005 scopus 로고    scopus 로고
    • The C15-lactone was formed as a minor product through oxidation of the C15-primary hydroxy group of 32 to the aldehyde, followed by further oxidation of the resultant C15-hemiacetal 31
    • The C15-lactone was formed as a minor product through oxidation of the C15-primary hydroxy group of 32 to the aldehyde, followed by further oxidation of the resultant C15-hemiacetal 31.
  • 85
    • 84911939880 scopus 로고    scopus 로고
    • The order of base addition was important for the regioselectivity. Bz2O and Et3N benzoylated the C9-OH of tetraol 36, and in situ addition of DMAP induced the benzoylation of the C8-OH
    • The order of base addition was important for the regioselectivity. Bz2O and Et3N benzoylated the C9-OH of tetraol 36, and in situ addition of DMAP induced the benzoylation of the C8-OH.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.