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Volumn 71, Issue 5, 2006, Pages 1809-1816

Concise synthesis of the neo-clerodane skeleton of teucrolivin A using a pericyclic reaction cascade

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOMER; PERICYCLIC REACTION;

EID: 33644657170     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052052i     Document Type: Article
Times cited : (23)

References (36)
  • 7
    • 0042814286 scopus 로고    scopus 로고
    • For examples of the stereoselective formation of quaternary carbons using the tandem pericyclic reaction, see: (a) Barriault, L.; Denissova, I. Org. Lett. 2002, 4, 1371.
    • (2002) Org. Lett. , vol.4 , pp. 1371
    • Barriault, L.1    Denissova, I.2
  • 14
    • 0001521888 scopus 로고
    • (f) Fuji, K. Chem. Rev. 1993, 93, 2037.
    • (1993) Chem. Rev. , vol.93 , pp. 2037
    • Fuji, K.1
  • 27
    • 33644648319 scopus 로고    scopus 로고
    • note
    • Any and all attempts at improving the efficiency of this transformation unfortunately did not result in any improvements in yield.
  • 28
    • 11144325118 scopus 로고    scopus 로고
    • For a review on microwaves in organic synthesis, see: (a) Kappe, C. O. Angew. Chem., Int. Ed. 2004, 43, 6250.
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 6250
    • Kappe, C.O.1
  • 34
    • 33644643065 scopus 로고    scopus 로고
    • note
    • Assuming that the stereochemistry of the anomeric center in the natural product is the thermodynamic isomer, we should observe the stereochemistry upon oxidative cleavage and subsequent cyclization should be equivalent to that seen in 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.