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Volumn , Issue 12, 2005, Pages 1560-1562

The first enantioselective total synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl ether

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ANTIINFECTIVE AGENT; PHTHALIDE DERIVATIVE; SPIROLAXINE METHYL ETHER; SULFONE; UNCLASSIFIED DRUG;

EID: 17444430743     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b418106a     Document Type: Article
Times cited : (45)

References (18)
  • 1
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    • M. J. Blaser, Clin. Infect. Dis., 1992, 15, 386; J. H. Walsh and W. L. Peterson, New England J. Med., 1995, 333, 984; B. Rathbone, Scrip Magazine, 1993, 25.
    • (1992) Clin. Infect. Dis. , vol.15 , pp. 386
    • Blaser, M.J.1
  • 2
    • 0029147865 scopus 로고
    • M. J. Blaser, Clin Infect. Dis., 1992, 15, 386; J. H. Walsh and W. L. Peterson, New England J. Med., 1995, 333, 984; B. Rathbone, Scrip Magazine, 1993, 25.
    • (1995) New England J. Med. , vol.333 , pp. 984
    • Walsh, J.H.1    Peterson, W.L.2
  • 3
    • 0026706766 scopus 로고
    • M. J. Blaser, Clin Infect. Dis., 1992, 15, 386; J. H. Walsh and W. L. Peterson, New England J. Med., 1995, 333, 984; B. Rathbone, Scrip Magazine, 1993, 25.
    • (1993) Scrip Magazine , pp. 25
    • Rathbone, B.1
  • 5
    • 17444405389 scopus 로고    scopus 로고
    • PCT Int. Appl., 1996, W0 9605204; CAN 125:58200
    • A. Arnone, G. Assante, G. Nasini and O. Vajna de Pava, Phytochemistry, 1990, 29, 613; M. A. Gaudliana, L. H. Huang, T. Kaneko and P. C. Watts, PCT Int. Appl., 1996, W0 9605204; CAN 125:58200.
    • Gaudliana, M.A.1    Huang, L.H.2    Kaneko, T.3    Watts, P.C.4
  • 10
    • 0001489687 scopus 로고
    • The absolute stereochemistry of 11 was confirmed as (R) by comparison of its optical rotation with that of the (S)-enantiomer as reported by Y. Mori, A. Takeuchi, H. Kageyama and M. Suzuki, Tetrahedron Lett., 1988, 29, 5423.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 5423
    • Mori, Y.1    Takeuchi, A.2    Kageyama, H.3    Suzuki, M.4
  • 12
    • 0028004542 scopus 로고
    • The effect of LiBr on acetylide addition reactions has been noted: P. E. van Rijn, S. Mommers, R. G. Visser, H. D. Verkruijsse and L. Brandsma, Synthesis, 1981, 451; E. M. Carreira and J. Du Bois. J. Am. Chem. Soc., 1994, 116, 10825.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 10825
    • Carreira, E.M.1    Du Bois, J.2
  • 13
    • 0003536850 scopus 로고
    • Pergamon Press, New York
    • For reviews on the anomeric effect see: P. Deslongchamps, Stereoelectronic Effects in Organic Chemistry, Pergamon Press, New York, 1983; A. J. Kirby, The Anomeric Effect and Related Stereoelectronic Effects at Oxygen, Springer-Verlag, New York, 1983.
    • (1983) Stereoelectronic Effects in Organic Chemistry
    • Deslongchamps, P.1
  • 17
    • 0034644036 scopus 로고    scopus 로고
    • For examples of the use of the heterocycle-activated modified Julia reaction using heterocyclic sulfones bearing a spiroacetal functionality see: S. V. Ley, A. C. Humphries, H. Eick, R. Downham, A. R. Ross, R. J. Boyce, J. B. J. Pavey and J. Pietruszka, J. Chem. Soc., Perkin Trans 1, 1998, 3907; T. Shimizu, T. Masuda, K. Hiramoto and T. Nakata, Org. Lett., 2000, 2, 2153.
    • (2000) Org. Lett. , vol.2 , pp. 2153
    • Shimizu, T.1    Masuda, T.2    Hiramoto, K.3    Nakata, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.