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Volumn 133, Issue 24, 2011, Pages 9216-9219

Convergent and stereodivergent synthesis of complex 1-aza-7-oxabicyclo[2.2. 1]heptanes

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC ALCOHOL; COUPLING REACTION; FUNCTIONALIZED; GLYOXYLATE; HOMOALLYLIC AMINES; INTRAMOLECULAR ANNULATION; N-OXIDATION; NITRONES; REACTION PATHWAYS; STEREODIVERGENT SYNTHESIS;

EID: 79959236161     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja202900h     Document Type: Article
Times cited : (20)

References (21)
  • 8
    • 0001516038 scopus 로고
    • For a discussion concerning the observation of products derived from aza-Cope/intramolecular [3 + 2] nitrone cycloaddition, see
    • For a discussion concerning the observation of products derived from aza-Cope/intramolecular [3 + 2] nitrone cycloaddition, see: Wuts, P. G. M.; Jung, Y.-W. J. Org. Chem. 1988, 53, 1957
    • (1988) J. Org. Chem. , vol.53 , pp. 1957
    • Wuts, P.G.M.1    Jung, Y.-W.2
  • 17
    • 34247106589 scopus 로고    scopus 로고
    • For a computational assessment related to the competition between [3,3] rearrangement and [3 + 2] cycloaddition reactions of homoallylic nitrones, see
    • For a computational assessment related to the competition between [3,3] rearrangement and [3 + 2] cycloaddition reactions of homoallylic nitrones, see: Merino, P.; Tejero, T.; Mannucci, V. Tetrahedron Lett. 2007, 48, 3385
    • (2007) Tetrahedron Lett. , vol.48 , pp. 3385
    • Merino, P.1    Tejero, T.2    Mannucci, V.3
  • 18
    • 79959211150 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.
  • 20
    • 0000789240 scopus 로고
    • It has also been proposed that intermolecular [3 + 2] cycloaddition reactions occur faster by way of (E)-nitrones. See:;;; J. Org. Chem. 1990, 55, 3427
    • Inouye, Y.; Takaya, K.; Kakisawa, H. Bull. Chem. Soc. Jpn. 1983, 56, 3541 It has also been proposed that intermolecular [3 + 2] cycloaddition reactions occur faster by way of (E)-nitrones. See: Burdisso, M.; Gandolfi, R.; Grünanger, P.; Rastelli, A. J. Org. Chem. 1990, 55, 3427
    • (1983) Bull. Chem. Soc. Jpn. , vol.56 , pp. 3541
    • Inouye, Y.1    Takaya, K.2    Kakisawa, H.3    Burdisso, M.4    Gandolfi, R.5    Grünanger, P.6    Rastelli, A.7
  • 21
    • 79959264337 scopus 로고    scopus 로고
    • These observations do not exclude control by the Curtin-Hammett principle, where reversible [3,3] rearrangement of the initially formed glyoxylate-based nitrone is irrelevant in determining the product distribution
    • These observations do not exclude control by the Curtin-Hammett principle, where reversible [3,3] rearrangement of the initially formed glyoxylate-based nitrone is irrelevant in determining the product distribution.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.