메뉴 건너뛰기




Volumn , Issue 9, 1997, Pages 1841-1851

Substrate-directed diastereoselective hydroformylations, 1: Substrate-directed diastereoselective hydroformylation of methallylic alcohols - Development of an efficient catalyst-directing group for rhodium-catalyzed hydroformylation

Author keywords

Asymmetric synthesis; Catalyst directing group; Homogeneous catalysis; Hydroformylations; Rhodium

Indexed keywords


EID: 0003719460     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970907     Document Type: Article
Times cited : (39)

References (56)
  • 11
    • 0016204729 scopus 로고
    • Selected examples of natural products containing the fragment 1: [4a] cis- and trans-whiskey lactones: K. Otsuka, Y. Zenibayashi, M. Itoh, Agr. Biol. Chem. 1974, 38, 485-490.
    • (1974) Agr. Biol. Chem. , vol.38 , pp. 485-490
    • Otsuka, K.1    Zenibayashi, Y.2    Itoh, M.3
  • 12
    • 0017615504 scopus 로고
    • [4b] K. Mori, Tetrahedron 1977, 33, 289-294.
    • (1977) Tetrahedron , vol.33 , pp. 289-294
    • Mori, K.1
  • 15
    • 0003891136 scopus 로고
    • (Ed.: J. V. Rodricks, C. V. Hesseltine, M. A. Mehlman), Pathotox Publ., Park Forest South, Il.
    • [4d] Verrucarin A: C. Tamm in Mycotoxins in Human and Animal Health (Ed.: J. V. Rodricks, C. V. Hesseltine, M. A. Mehlman), Pathotox Publ., Park Forest South, Il., 1977, p. 209.
    • (1977) Mycotoxins in Human and Animal Health , pp. 209
    • Tamm, C.1
  • 17
  • 24
    • 0000877148 scopus 로고
    • For a review see: J. M. Brown, Angew. Chem. 1987, 99, 169-182;
    • (1987) Angew. Chem. , vol.99 , pp. 169-182
    • Brown, J.M.1
  • 27
    • 0343566234 scopus 로고
    • (Ed.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart
    • For a review on stereoselective hydroformylations see: [11a] P. Eilbracht in Houben-Weyl, Methods of Organic Synthesis, E 21c, Stereoselective Synthesis, (Ed.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, 1995, p. 2488-2558.
    • (1995) Houben-Weyl, Methods of Organic Synthesis, E 21c, Stereoselective Synthesis , pp. 2488-2558
    • Eilbracht, P.1
  • 28
    • 0001247486 scopus 로고
    • For substrate-directed diastereoselective hydroformylation of cyclic systems see: [11b] S. D. Burke, J. E. Cobb, Tetrahedron Lett. 1986, 27, 4237-4240.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 4237-4240
    • Burke, S.D.1    Cobb, J.E.2
  • 31
    • 0000680768 scopus 로고    scopus 로고
    • Parts of this work have been published previously as a preliminary communication: B. Breit, Angew. Chem. 1996, 108, 3021-3023;
    • (1996) Angew. Chem. , vol.108 , pp. 3021-3023
    • Breit, B.1
  • 35
    • 0001854915 scopus 로고    scopus 로고
    • For the use of rhodium hydroformylation catalysts modified with stronc π-acceptor ligands see: B. Breit, J. Chem. Soc., Chem. Commun. 1996, 2071-2072.
    • (1996) J. Chem. Soc., Chem. Commun. , pp. 2071-2072
    • Breit, B.1
  • 36
    • 37049078963 scopus 로고
    • J. M. Brown, A. G. Kent, J. Chem. Soc., Perkin Trans. 2 1987, 1597-1607. A bidentate ligand would not be suited here; because of the chelate effect the binding constant would be too large.
    • (1987) J. Chem. Soc., Perkin Trans. 2 , pp. 1597-1607
    • Brown, J.M.1    Kent, A.G.2
  • 41
  • 55
    • 33748722601 scopus 로고    scopus 로고
    • note
    • Although these products gave clean NMR spectra, correct elemental analyses could not be obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.