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Volumn 10, Issue 9, 2008, Pages 1786-1790

Enantioselective synthesis of iridal, the parent molecule of the iridal triterpenoid class

Author keywords

[No Author keywords available]

Indexed keywords

IRIDAL; PALLADIUM; TRITERPENE;

EID: 48349107034     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8005425     Document Type: Article
Times cited : (9)

References (27)
  • 12
    • 58149198940 scopus 로고    scopus 로고
    • The constant structural motif in the iridal series is the central six-membered B-ring, incorporating two adjacent quaternary centers at C10, C11. The same ring system, albeit with different locations of unsaturation and oxygen functionality, is found in a great number of related molecules.
    • The constant structural motif in the iridal series is the central six-membered B-ring, incorporating two adjacent quaternary centers at C10, C11. The same ring system, albeit with different locations of unsaturation and oxygen functionality, is found in a great number of related molecules.
  • 13
    • 7044235263 scopus 로고    scopus 로고
    • (a) Tietze, L. F. Chem. Rev. 1996, 96. 115-136.
    • (1996) Chem. Rev , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 14
    • 0001847186 scopus 로고    scopus 로고
    • Shibasaki, M, Stoddart, J. F, Vogtle, F, Eds, Wiley-VCH: Weinheim, Germany
    • (b) Tietze, L. F.; Haunert, F. In Stimulating Concepts in Chemistry; Shibasaki, M., Stoddart, J. F., Vogtle, F., Eds.; Wiley-VCH: Weinheim, Germany, 2000; pp 39-64.
    • (2000) Stimulating Concepts in Chemistry , pp. 39-64
    • Tietze, L.F.1    Haunert, F.2
  • 15
    • 84890766709 scopus 로고    scopus 로고
    • Tietze, L. F, Brasche, G, Gericke. K. M, Eds, Wiley-VCH: Weinheim, Germany, ISBN: 3-527-29060-5
    • (c) Domino Reactions In Organic Synthesis.; Tietze, L. F., Brasche, G., Gericke. K. M., Eds.: Wiley-VCH: Weinheim, Germany, 2006; ISBN: 3-527-29060-5.
    • (2006) Domino Reactions In Organic Synthesis
  • 17
    • 58149184491 scopus 로고    scopus 로고
    • Both quaternary stereogenic centers are obtained as required; no stereoisomer formation was detected
    • Both quaternary stereogenic centers are obtained as required; no stereoisomer formation was detected.
  • 22
    • 58149195588 scopus 로고    scopus 로고
    • For the original procedure (reduction of acrylonitriles) see: Profitt, J. A.; Watt, D. S.; Corey, E. J. J. Org. Chem. 1975, 40, 127. Adapted to α,ß,-unsaturated esters by: Hudlicky, T.; Sinai-Zingde, G.; Natchus, M. G. Tetrahedron Lett. 1987, 28, 5287-5290.
    • For the original procedure (reduction of acrylonitriles) see: Profitt, J. A.; Watt, D. S.; Corey, E. J. J. Org. Chem. 1975, 40, 127. Adapted to α,ß,-unsaturated esters by: Hudlicky, T.; Sinai-Zingde, G.; Natchus, M. G. Tetrahedron Lett. 1987, 28, 5287-5290.
  • 24
    • 85082860156 scopus 로고
    • and references cited therein
    • Negishi, E.; Takahashi, T. Synthesis 19881 - 19, and references cited therein.
    • (1988) Synthesis , pp. 1-19
    • Negishi, E.1    Takahashi, T.2
  • 26
    • 2042507954 scopus 로고    scopus 로고
    • Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483. Chemler, S. R.; Trauner, D.; Danishevsky, S. Angew. Chem., Int. Ed. 2001, 40, 4544-4568.
    • Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483. Chemler, S. R.; Trauner, D.; Danishevsky, S. Angew. Chem., Int. Ed. 2001, 40, 4544-4568.
  • 27
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    • 7.2 E double bond are known: Takahashi, K.; Suzuki, S.; Hano. Y.; Nomura, T. Biol. Pharm. Bull. 2002, 25, 432-436.
    • 7.2 E double bond are known: Takahashi, K.; Suzuki, S.; Hano. Y.; Nomura, T. Biol. Pharm. Bull. 2002, 25, 432-436.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.