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Volumn 73, Issue 11, 2008, Pages 4139-4150

Total synthesis of solandelactones A, B, E, and F exploiting a tandem petasis-claisen lactonization strategy

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; CHEMICAL REACTIONS; ETHERS; MICROFLUIDICS; ORGANIC COMPOUNDS; SET THEORY;

EID: 44949142206     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800335g     Document Type: Article
Times cited : (45)

References (50)
  • 4
    • 0029107374 scopus 로고
    • and references cited therein
    • (c) Faulkner, D. J. Nat. Prod. Rep. 1995, 12, 223. and references cited therein.
    • (1995) Nat. Prod. Rep , vol.12 , pp. 223
    • Faulkner, D.J.1
  • 18
    • 0032568128 scopus 로고    scopus 로고
    • For an earlier approach to the synthesis of this portion of solandelactones, see: a
    • For an earlier approach to the synthesis of this portion of solandelactones, see: (a) Varadarajan, S.; Mohapatra, D. K.; Datta, A. Tetrahedron Lett. 1998, 39, 1075.
    • (1998) Tetrahedron Lett , vol.39 , pp. 1075
    • Varadarajan, S.1    Mohapatra, D.K.2    Datta, A.3
  • 25
    • 0032573530 scopus 로고    scopus 로고
    • For other routes to 13, see: (a) Da Silva, C. B.; Pale, P Tetrahedron: Asymmetry 1998, 9, 3951.
    • For other routes to 13, see: (a) Da Silva, C. B.; Pale, P Tetrahedron: Asymmetry 1998, 9, 3951.
  • 35
    • 44949189054 scopus 로고    scopus 로고
    • A possible explanation for this failure lies in the barrier, estimated to be 7.9 kcal/mol by a Hartree-Fock/6-31G** calculation, for conversion of the more stables trans ester conformation to s-cis conformation 72 required for RCM.
    • A possible explanation for this failure lies in the barrier, estimated to be 7.9 kcal/mol by a Hartree-Fock/6-31G** calculation, for conversion of the more stables trans ester conformation to s-cis conformation 72 required for RCM.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.