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Volumn 131, Issue 20, 2009, Pages 6932-6933

Rh-catalyzed intramolecular olefin hydroacylation: Enantioselective synthesis of seven- And eight-membered heterocycles

Author keywords

[No Author keywords available]

Indexed keywords

C-H BOND; ENANTIOCONTROL; ENANTIOSELECTIVE SYNTHESIS; FUNCTIONALIZATIONS; HETEROCYCLES; HYDROACYLATION; ISOTOPIC LABELING; LIMITING STEP; REDUCTIVE ELIMINATION; RHODIUM-CATALYZED; STEREO-SELECTIVE; SUBSTRATE STRUCTURE;

EID: 70149090116     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja901915u     Document Type: Article
Times cited : (160)

References (26)
  • 1
    • 30744476469 scopus 로고    scopus 로고
    • For reviews on medium-sized rings in natural products, see: (a) Inoue, M. Chem. Rev. 2005, 105, 4379-4405.
    • (2005) Chem. Rev. , vol.105 , pp. 4379-4405
    • Inoue, M.1
  • 2
    • 33846870797 scopus 로고    scopus 로고
    • (b) Shiina, I. Chem. Rev. 2007, 107, 239-273.
    • (2007) Chem. Rev. , vol.107 , pp. 239-273
    • Shiina, I.1
  • 4
    • 0034246704 scopus 로고    scopus 로고
    • Yet, L. Chem. Rev. 2000, 100, 2963-3007.
    • (2000) Chem. Rev. , vol.100 , pp. 2963-3007
    • Yet, L.1
  • 5
    • 67749086553 scopus 로고    scopus 로고
    • For rare examples of transition-metal-catalyzed enantioselective mediumring synthesis, see: Watson, I. D. G.; Ritter, S.; Toste, F. D. J. Am. Chem. Soc. 2009, 131, 2056-2057, and references therein.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 2056-2057
    • Watson, I.D.G.1    Ritter, S.2    Toste, F.D.3
  • 6
    • 84890779821 scopus 로고    scopus 로고
    • Evans, P. A., Ed.; Wiley-VCH: New York
    • For a review of hydroacylation, see: Fu, G. C. In Modern RhodiumCatalyzed Organic Reactions; Evans, P. A., Ed.; Wiley-VCH: New York, 2005; pp 79-91, and references therein.
    • (2005) Modern RhodiumCatalyzed Organic Reactions , pp. 79-91
    • Fu, G.C.1
  • 14
    • 70349125764 scopus 로고    scopus 로고
    • 3Cl, but an analogous oxygen-containing alkenal was unreactive (see ref 6a)
    • 3Cl, but an analogous oxygen-containing alkenal was unreactive (see ref 6a).
  • 18
    • 70349110408 scopus 로고    scopus 로고
    • It should be noted that this regioselectivity is opposite to that observed with oxygen-containing substrates 1a-g (Table 1)
    • It should be noted that this regioselectivity is opposite to that observed with oxygen-containing substrates 1a-g (Table 1).
  • 19
    • 70349115509 scopus 로고    scopus 로고
    • In the presence of (R)-DTBM-SEGPHOS, alkenals 5 and 6 undergo hydroacylation to produce the same enantiomer of 12
    • In the presence of (R)-DTBM-SEGPHOS, alkenals 5 and 6 undergo hydroacylation to produce the same enantiomer of 12.
  • 20
    • 0141508049 scopus 로고    scopus 로고
    • For applications of sulfoxides in transition-metal catalysis, see: Fernández, I.; Khiar, N. Chem. Rev. 2003, 103, 3651-3705.
    • (2003) Chem. Rev. , vol.103 , pp. 3651-3705
    • Fernández, I.1    Khiar, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.