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Volumn 110, Issue 5, 1988, Pages 1539-1546

Chiral Synthesis via Organoboranes. 14. Selective Reductions. 41. Diisopinocampheylchloroborane, an Exceptionally Efficient Chiral Reducing Agent

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EID: 0010176851     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00213a030     Document Type: Article
Times cited : (341)

References (54)
  • 2
    • 0000681818 scopus 로고
    • Reference 2, Vol. 2, Chapters 2–4. We have recently reported a survey on various chiral reducing agents and classified the reagents according to their capability to reduce certain standard classes of ketones The percent ee reported here for trans-4-phenyl-3-buten-2-one has been corrected to 81% ee from the earlier value of 12%
    • Reference 2, Vol. 2, Chapters 2–4. We have recently reported a survey on various chiral reducing agents and classified the reagents according to their capability to reduce certain standard classes of ketones: Brown, H. C.; Park, W. S.; Cho, B. T.; Ramachandran, P. V. J. Org. Chem. 1987, 52, 5406. The percent ee reported here for trans-4-phenyl-3-buten-2-one has been corrected to 81% ee from the earlier value of 12%.
    • (1987) J. Org. Chem. , vol.52 , pp. 5406
    • Brown, H.C.1    Park, W.S.2    Cho, B.T.3    Ramachandran, P.V.4
  • 4
  • 6
    • 0001381075 scopus 로고
    • (b) Kagan, G. B.; Fiaud, J. C. Top. Stereochem. 1978, 10, 175. For an extremely efficient borohydride reagent for chiral reduction, see: Brown, H. C.; Park, W. S.; Cho, B. T. J. Org. Chem. 1986, 51, 1934. Brown, H. C.; Cho, B. T.; Park, W. S. J. Org. Chem. 1986, 51, 3396
    • Haubenstock, H. Top. Stereochem. 1983, 14, 231. (b) Kagan, G. B.; Fiaud, J. C. Top. Stereochem. 1978, 10, 175. For an extremely efficient borohydride reagent for chiral reduction, see: Brown, H. C.; Park, W. S.; Cho, B. T. J. Org. Chem. 1986, 51, 1934. Brown, H. C.; Cho, B. T.; Park, W. S. J. Org. Chem. 1986, 51, 3396.
    • (1983) Top. Stereochem. , vol.14 , pp. 231
    • Haubenstock, H.1
  • 8
    • 0000679455 scopus 로고
    • R. Scheffold, Ed.; Springer-Verlag: Berlin (b) Srebnik, M.; Ramachandran, P. V. Aldrichimica Acta 1987, 20, 9
    • (a) Brown, H. C.; Jadhav, P. K.; Singaram, B. In Modern Synthetic Methods; R. Scheffold, Ed.; Springer-Verlag: Berlin 1986; Vol. 4, p 307. (b) Srebnik, M.; Ramachandran, P. V. Aldrichimica Acta 1987, 20, 9.
    • (1986) Modern Synthetic Methods , vol.4 , pp. 307
    • Brown, H.C.1    Jadhav, P.K.2    Singaram, B.3
  • 9
    • 85022546418 scopus 로고    scopus 로고
    • Reference 2
    • Chapter 1
    • Brown, H. C.; Jadhav, P. K., Reference 2, Vol 2, Chapter 1.
    • , vol.2
    • Brown, H.C.1    Jadhav, P.K.2
  • 27
    • 0000031679 scopus 로고
    • For a paper on a related compound from nopol methyl ether and monochloroborane, see
    • For a paper on a related compound from nopol methyl ether and monochloroborane, see: Shiner, C. S.; Garner, C. M.; Haltiwanger, R. C. J. Am. Chem. Soc. 1985, 107, 7167.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 7167
    • Shiner, C.S.1    Garner, C.M.2    Haltiwanger, R.C.3
  • 29
    • 85012324558 scopus 로고    scopus 로고
    • manuscript in preparation
    • Oberlander, R. A.; Nichols, D. E.; Ramachandran, P. V.; Srebnik, M. J. Pharm. Pharmacol., in press
    • Srebnik, M., Ramachandran, P. V.; Brown, H. C., manuscript in preparation. Oberlander, R. A.; Nichols, D. E.; Ramachandran, P. V.; Srebnik, M. J. Pharm. Pharmacol., in press.
    • Srebnik, M.1    Ramachandran, P.V.2    Brown, H.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.