메뉴 건너뛰기




Volumn 61, Issue 12, 1996, Pages 4151-4153

Biocatalytic syntheses of protected D-mannose-d5, D-mannose-d7, D-mannitol-2,3,4,5,6-d5, and D-mannitol-1,1,2,3,4,5,6,6-d8

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001144206     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951666s     Document Type: Article
Times cited : (23)

References (38)
  • 11
    • 4243057281 scopus 로고    scopus 로고
    • note
    • (d) This sugar is available commercially.
  • 12
    • 4243125315 scopus 로고    scopus 로고
    • University of Arizona, private communication
    • Gervay, J., University of Arizona, private communication.
    • Gervay, J.1
  • 13
    • 0002485317 scopus 로고
    • For recent reviews concerning halocyclohexadiene-cis-diols, see: (a) Hudlicky, T.; Reed, J. W. Adv. Asymm. Synth. 1995, 1, 271. (b) Brown, S. M.; Hudlicky, T. In Organic Synthesis: Theory and Practice; Hudlicky, T., Ed; JAI Press: Greenwich, CT, 1992; Vol. 2, p 113. (c) Carless, H. A. J. Tetrahedron: Asymmetry 1992, 795. (d) Widdowson, D. A.; Ribbons, D. A.; Thomas, S. D. Janssen Chim. Acta 1990, 8, 3.
    • (1995) Adv. Asymm. Synth. , vol.1 , pp. 271
    • Hudlicky, T.1    Reed, J.W.2
  • 14
    • 0001345541 scopus 로고
    • Hudlicky, T., Ed; JAI Press: Greenwich, CT
    • For recent reviews concerning halocyclohexadiene-cis-diols, see: (a) Hudlicky, T.; Reed, J. W. Adv. Asymm. Synth. 1995, 1, 271. (b) Brown, S. M.; Hudlicky, T. In Organic Synthesis: Theory and Practice; Hudlicky, T., Ed; JAI Press: Greenwich, CT, 1992; Vol. 2, p 113. (c) Carless, H. A. J. Tetrahedron: Asymmetry 1992, 795. (d) Widdowson, D. A.; Ribbons, D. A.; Thomas, S. D. Janssen Chim. Acta 1990, 8, 3.
    • (1992) Organic Synthesis: Theory and Practice , vol.2 , pp. 113
    • Brown, S.M.1    Hudlicky, T.2
  • 15
    • 1542392363 scopus 로고
    • For recent reviews concerning halocyclohexadiene-cis-diols, see: (a) Hudlicky, T.; Reed, J. W. Adv. Asymm. Synth. 1995, 1, 271. (b) Brown, S. M.; Hudlicky, T. In Organic Synthesis: Theory and Practice; Hudlicky, T., Ed; JAI Press: Greenwich, CT, 1992; Vol. 2, p 113. (c) Carless, H. A. J. Tetrahedron: Asymmetry 1992, 795. (d) Widdowson, D. A.; Ribbons, D. A.; Thomas, S. D. Janssen Chim. Acta 1990, 8, 3.
    • (1992) Tetrahedron: Asymmetry , pp. 795
    • Carless, H.A.J.1
  • 16
    • 0002748323 scopus 로고
    • For recent reviews concerning halocyclohexadiene-cis-diols, see: (a) Hudlicky, T.; Reed, J. W. Adv. Asymm. Synth. 1995, 1, 271. (b) Brown, S. M.; Hudlicky, T. In Organic Synthesis: Theory and Practice; Hudlicky, T., Ed; JAI Press: Greenwich, CT, 1992; Vol. 2, p 113. (c) Carless, H. A. J. Tetrahedron: Asymmetry 1992, 795. (d) Widdowson, D. A.; Ribbons, D. A.; Thomas, S. D. Janssen Chim. Acta 1990, 8, 3.
    • (1990) Janssen Chim. Acta , vol.8 , pp. 3
    • Widdowson, D.A.1    Ribbons, D.A.2    Thomas, S.D.3
  • 35
    • 4243098358 scopus 로고    scopus 로고
    • note
    • Diol 2b is derived from perdeuteriobromobenzene which was obtained from Genencor International.
  • 37
    • 85086288660 scopus 로고    scopus 로고
    • note
    • 4) reductions also led to the cleavage of one of the silyl protecting groups, although it is not clear from the spectroscopic evidence which one.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.