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Volumn 15, Issue 13, 2013, Pages 3330-3333

Approach to the tricyclic core of the tigliane-daphnane diterpenes. Concerning the utility of transannular aldol additions

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; DITERPENE; MEZEREIN;

EID: 84880033159     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401367h     Document Type: Article
Times cited : (37)

References (32)
  • 2
    • 85007767611 scopus 로고
    • For synthetic approaches to the 5-7-6 ring system, see: Kogen, H. J. Syn. Org. Chem. Jpn. 1990, 48, 724
    • (1990) J. Syn. Org. Chem. Jpn. , vol.48 , pp. 724
    • Kogen, H.1
  • 25
    • 0010521593 scopus 로고
    • For conjugate reduction with L-Selectride as a means of enolate formation, see: Fortunato, J. M.; Ganem, B. J. Org. Chem. 1976, 41, 2194
    • (1976) J. Org. Chem. , vol.41 , pp. 2194
    • Fortunato, J.M.1    Ganem, B.2
  • 26
    • 0000975755 scopus 로고    scopus 로고
    • 6) was also effective as a hydride source. For reductive aldol reactions with Stryker's reagent, see: Chiu, P.; Szeto, C.-P.; Geng, Z.; Cheng, K.-F. Org. Lett. 2001, 3, 1901
    • (2001) Org. Lett. , vol.3 , pp. 1901
    • Chiu, P.1    Szeto, C.-P.2    Geng, Z.3    Cheng, K.-F.4
  • 27
    • 36749062886 scopus 로고    scopus 로고
    • Conjugate reduction with L-Selectride favors the formation of a lithium enolate as opposed to a boron enolate. The yield of boron enolate, however, has been shown to be highly dependent on the alkali-metal cation in the order of K > Na > Li; see: Ma, L.; Hopson, R.; Li, D.; Zhang, Y.; Williard, P. G. Organometallics 2007, 26, 5834
    • (2007) Organometallics , vol.26 , pp. 5834
    • Ma, L.1    Hopson, R.2    Li, D.3    Zhang, Y.4    Williard, P.G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.