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Volumn 12, Issue 11, 2010, Pages 2528-2531

Rh(I)-catalyzed [(3 + 2) + 1] cycloaddition of 1-yne/ene-vinylcyclopropanes and CO: Homologous pauson-khand reaction and total synthesis of (±)-α-agarofuran

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AGAROFURAN; ALPHA-AGAROFURAN; CYCLOPROPANE DERIVATIVE; RHODIUM; SESQUITERPENE;

EID: 77952964640     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100625e     Document Type: Article
Times cited : (117)

References (53)
  • 1
    • 77953001655 scopus 로고    scopus 로고
    • Recent reviews on the Diels-Alder reaction
    • Recent reviews on the Diels-Alder reaction
  • 10
    • 77953000330 scopus 로고    scopus 로고
    • note
    • We suggest here a new nomenclature for the two-component cycloaddition of an ene/yne-VCP substrate and CO. It is referred to as [(3 + 2) + 1] cycloaddition, where the "3 + 2" part comes from one molecule, the "1" part comes from another molecule.
  • 11
    • 77953015158 scopus 로고    scopus 로고
    • Selected reviews on the Pauson-Khand reaction
    • Selected reviews on the Pauson-Khand reaction
  • 16
    • 77952978690 scopus 로고    scopus 로고
    • Selected recent reports on cyclopropane participating cycloaddition reactions
    • Selected recent reports on cyclopropane participating cycloaddition reactions
  • 32
    • 77953011424 scopus 로고    scopus 로고
    • note
    • The vinyl group activation strategy was also demonstrated by Wender's group in [2 + 2+ 1] cycloaddition reactions; see
  • 37
    • 77952998270 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see
  • 40
    • 77953015157 scopus 로고    scopus 로고
    • note
    • 2-catalyzed Pauson-Khand reaction was also found to be optimal under low CO pressure, see
  • 42
    • 77953013581 scopus 로고    scopus 로고
    • note
    • We also attempted the [(3 + 2) + 1] reaction of a 1-ene-VCP substrate with elongated tether. Unfortunetely, the reaction afforded a complex mixture, and no corresponding 6,6-bicyclic cyclohexanone product was isolated.
  • 46
    • 77952974583 scopus 로고    scopus 로고
    • note
    • The [(3 + 2) + 1] cycloaddition of gem -diester-tethered substrate 23 was also conducted under identical conditions. However, the reaction was very sluggish, and the yield was unsatisfactory.
  • 49
    • 77953018344 scopus 로고    scopus 로고
    • Reports on α-agarofuran synthesis
    • Reports on α-agarofuran synthesis


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.