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Volumn 7, Issue 4, 2005, Pages 569-572

An expeditious synthesis of DPD and boron binding studies

Author keywords

[No Author keywords available]

Indexed keywords

4,5 DIHYDROXYPENTANE 2,3 DIONE; BORIC ACID; HYDROXYL GROUP; KETONE; PENTANE; UNCLASSIFIED DRUG;

EID: 14844363497     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol047695j     Document Type: Article
Times cited : (115)

References (22)
  • 10
    • 14844347589 scopus 로고    scopus 로고
    • For full data, see Supporting Information
    • For full data, see Supporting Information.
  • 11
    • 0026623543 scopus 로고
    • Isopropylidene glyceraldehyde can be generated as either enantiomer in a few steps, but it is quite volatile and dimerizes readily. These drawbacks have led to the development of other protecting groups for glyceraldehyde. (a) For a general discussion, see: Schmid, C. R.; Bradley, D. A. Synthesis 1992, 587-590. (b) For discussion and elaborate solutions, see: Michel, P.; Ley, S. V. Synthesis 2003, 10, 1598-1602. Aube, J.; Mossman, C. J.; Dickey, S. Tetrahedron 1992, 48, 45, 9819-9826. (c) First reported by: Grauert, M.; Schollkopf, U. Liebigs, Ann. Chem. 1985, 1817-1824
    • (1992) Synthesis , pp. 587-590
    • Schmid, C.R.1    Bradley, D.A.2
  • 12
    • 0042243690 scopus 로고    scopus 로고
    • Isopropylidene glyceraldehyde can be generated as either enantiomer in a few steps, but it is quite volatile and dimerizes readily. These drawbacks have led to the development of other protecting groups for glyceraldehyde. (a) For a general discussion, see: Schmid, C. R.; Bradley, D. A. Synthesis 1992, 587-590. (b) For discussion and elaborate solutions, see: Michel, P.; Ley, S. V. Synthesis 2003, 10, 1598-1602. Aube, J.; Mossman, C. J.; Dickey, S. Tetrahedron 1992, 48, 45, 9819-9826. (c) First reported by: Grauert, M.; Schollkopf, U. Liebigs, Ann. Chem. 1985, 1817-1824
    • (2003) Synthesis , vol.10 , pp. 1598-1602
    • Michel, P.1    Ley, S.V.2
  • 13
    • 0026489676 scopus 로고
    • Isopropylidene glyceraldehyde can be generated as either enantiomer in a few steps, but it is quite volatile and dimerizes readily. These drawbacks have led to the development of other protecting groups for glyceraldehyde. (a) For a general discussion, see: Schmid, C. R.; Bradley, D. A. Synthesis 1992, 587-590. (b) For discussion and elaborate solutions, see: Michel, P.; Ley, S. V. Synthesis 2003, 10, 1598-1602. Aube, J.; Mossman, C. J.; Dickey, S. Tetrahedron 1992, 48, 45, 9819-9826. (c) First reported by: Grauert, M.; Schollkopf, U. Liebigs, Ann. Chem. 1985, 1817-1824
    • (1992) Tetrahedron , vol.48 , Issue.45 , pp. 9819-9826
    • Aube, J.1    Mossman, C.J.2    Dickey, S.3
  • 14
    • 84985231751 scopus 로고
    • Isopropylidene glyceraldehyde can be generated as either enantiomer in a few steps, but it is quite volatile and dimerizes readily. These drawbacks have led to the development of other protecting groups for glyceraldehyde. (a) For a general discussion, see: Schmid, C. R.; Bradley, D. A. Synthesis 1992, 587-590. (b) For discussion and elaborate solutions, see: Michel, P.; Ley, S. V. Synthesis 2003, 10, 1598-1602. Aube, J.; Mossman, C. J.; Dickey, S. Tetrahedron 1992, 48, 45, 9819-9826. (c) First reported by: Grauert, M.; Schollkopf, U. Liebigs, Ann. Chem. 1985, 1817-1824
    • (1985) Liebigs, Ann. Chem. , pp. 1817-1824
    • Grauert, M.1    Schollkopf, U.2
  • 18
    • 0242299248 scopus 로고    scopus 로고
    • Pei and co-workers proposed that the C-3 carbonyl of DPD (enzymatically prepared) was hydrated in aqueous media: Zhu, J. G.; Hu, X. B.; Dizin, E.; Pei, D. H. J. Am. Chem. Soc. 2003, 125, 13379-13381.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 13379-13381
    • Zhu, J.G.1    Hu, X.B.2    Dizin, E.3    Pei, D.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.