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Volumn 125, Issue 38, 2003, Pages 11514-11515

Synthesis of (-)-terpestacin via catalytic, stereoselective fragment coupling: Siccanol is terpestacin, not 11-epi-terpestacin

Author keywords

[No Author keywords available]

Indexed keywords

11 EPITERPESTACIN; NATURAL PRODUCT; SESTERTERPENE; SICCANOL; TERPESTACIN; UNCLASSIFIED DRUG;

EID: 0141757454     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0373925     Document Type: Article
Times cited : (75)

References (29)
  • 25
    • 0141492899 scopus 로고    scopus 로고
    • note
    • -P-phenyl-P-(p-xylyl)-ferrocenylphosphine provided a higher overall yield (85%; 2.1:1 dr, 2.6:1 regioselectivity); see Supporting Information.
  • 26
    • 0141827566 scopus 로고    scopus 로고
    • note
    • Sodium hydroxide, finely dispersed in toluene, is likely the operative base, and it should be noted that the use of solvents other than toluene led to nearly exclusive O-alkylation of the enolate.
  • 28
    • 0141492898 scopus 로고    scopus 로고
    • note
    • epi-Terpestacin (1b) was prepared by the same sequence from 11-epi-13. The same nOe shown for 16 (Scheme 2) was observed in 11-epi-16.
  • 29
    • 0141716233 scopus 로고    scopus 로고
    • note
    • D, which Myers demonstrated to be artifactual (see ref 5).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.