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Volumn 4, Issue 14, 2002, Pages 2357-2360

Double diastereoselective intramolecular cyclopropanation to P-chiral [3.1.0]-bicyclic phosphonates

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; PHOSPHINE OXIDE DERIVATIVE;

EID: 0037062895     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026080o     Document Type: Article
Times cited : (26)

References (52)
  • 6
    • 0032562612 scopus 로고    scopus 로고
    • For reviews on the asymmetric synthesis of phosphorus compounds, including P-chiral phosphorus compounds, see: (a) Kolodiazhnyi, O. I. Tetrahedron: Asymmetry 1998, 9, 1279-1332.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 1279-1332
    • Kolodiazhnyi, O.I.1
  • 7
    • 12044254595 scopus 로고
    • (b) Pietrusiewicz, K. M.; Zablocka, M. Chem. Rev. 1994, 94, 1375-1411. For recent examples of the synthesis and use of P-chiral compounds, see:
    • (1994) Chem. Rev. , vol.94 , pp. 1375-1411
    • Pietrusiewicz, K.M.1    Zablocka, M.2
  • 22
    • 0032485248 scopus 로고    scopus 로고
    • and references therein
    • (a) Moody, C. J.; Miller, D. J. Tetrahedron 1998, 54, 2257-2268 and references therein. For the use of a-diazophosphonates as reagents in organic synthesis, see:
    • (1998) Tetrahedron , vol.54 , pp. 2257-2268
    • Moody, C.J.1    Miller, D.J.2
  • 28
    • 0041494783 scopus 로고    scopus 로고
    • For a review containing examples of intermolecular cyclopropanation reactions of α-diazophosphonates
    • (c) For a review containing examples of intermolecular cyclopropanation reactions of α-diazophosphonates, see:
  • 30
    • 0042496590 scopus 로고    scopus 로고
    • note
    • Note: the corresponding four enantiomeric conformations resulting from si-face attack of the rhodium carbene are not shown. The re-face of the carbene is defined as follows: (Matrix Presented)
  • 33
    • 0028799792 scopus 로고
    • For reviews of both diastereotopic and enantiotopic differentiation, see: (a) Magnuson, S. R. Tetrahedron 1995, 51, 2167-2213.
    • (1995) Tetrahedron , vol.51 , pp. 2167-2213
    • Magnuson, S.R.1
  • 41
    • 0041494784 scopus 로고    scopus 로고
    • See ref 10
    • (c) See ref 10.
  • 47
    • 0041995769 scopus 로고    scopus 로고
    • 31P analysis of the menthol-based systems
    • 31P analysis of the menthol-based systems.
  • 50
    • 0042496589 scopus 로고    scopus 로고
    • note
    • 3N and distilled under vacuum.
  • 51
    • 0041995768 scopus 로고    scopus 로고
    • note
    • R diastereomer is demonstrated, coelution with the trans diastereomers during flash chromatography hinders facile purification (see Supporting Information).
  • 52
    • 0042997396 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.