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Volumn 119, Issue 24, 1997, Pages 5512-5518

Stereocontrolled synthesis of a nonracemic vitamin B12 A-B semicorrin

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; SEMICORRIN; SULFIDE; UNCLASSIFIED DRUG;

EID: 0030801377     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9700515     Document Type: Article
Times cited : (26)

References (43)
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    • (1977) Science , vol.196 , pp. 1410-1420
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    • VCH: Weinheim, Germany
    • (d) Eschenmoser, A.; Winter, C. E Science 1977, 196, 1410-1420. For a brilliant review, see: Nicolaou, K. C.; Sorensen, E. J. Classics in Total Synthesis; VCH: Weinheim, Germany, 1996; pp 99-136.
    • (1996) Classics in Total Synthesis , pp. 99-136
    • Nicolaou, K.C.1    Sorensen, E.J.2
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    • 1842348542 scopus 로고    scopus 로고
    • Assigned from NOEDS measurements
    • Assigned from NOEDS measurements.
  • 34
    • 0001262182 scopus 로고
    • 12: Blanche, B.; Cameron, B.; Crouzet, J.; Debussche, L.; Thibaut, D.; Vuilhorgne, M.; Leeper, F. J.; Battersby, A. R. Angew. Chem. 1995, 107, 421-452. The oxidative sequence shown in Scheme 9 was first described by: Spencer, J. B.; Stolowich, N. J.; Roessner, C. A.; Min, C.; Scott, A. I. J. Am. Chem. Soc. 1993, 115, 11610-11611. The configuration at C-20 (tertiary alcohol) of precorrin-3x was assigned by: J. B.; Stolowich, N. J.; Wang, J.; Spencer, J. B.; Santander, P. J.; Roessner, C. A.; Scott, A. I. J. Am. Chem. Soc. 1996, 118, 1657-1662.
    • (1995) Angew. Chem. , vol.107 , pp. 421-452
    • Blanche, B.1    Cameron, B.2    Crouzet, J.3    Debussche, L.4    Thibaut, D.5    Vuilhorgne, M.6    Leeper, F.J.7    Battersby, A.R.8
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    • 12: Blanche, B.; Cameron, B.; Crouzet, J.; Debussche, L.; Thibaut, D.; Vuilhorgne, M.; Leeper, F. J.; Battersby, A. R. Angew. Chem. 1995, 107, 421-452. The oxidative sequence shown in Scheme 9 was first described by: Spencer, J. B.; Stolowich, N. J.; Roessner, C. A.; Min, C.; Scott, A. I. J. Am. Chem. Soc. 1993, 115, 11610-11611. The configuration at C-20 (tertiary alcohol) of precorrin-3x was assigned by: J. B.; Stolowich, N. J.; Wang, J.; Spencer, J. B.; Santander, P. J.; Roessner, C. A.; Scott, A. I. J. Am. Chem. Soc. 1996, 118, 1657-1662.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 11610-11611
    • Spencer, J.B.1    Stolowich, N.J.2    Roessner, C.A.3    Min, C.4    Scott, A.I.5
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    • J. B.
    • 12: Blanche, B.; Cameron, B.; Crouzet, J.; Debussche, L.; Thibaut, D.; Vuilhorgne, M.; Leeper, F. J.; Battersby, A. R. Angew. Chem. 1995, 107, 421-452. The oxidative sequence shown in Scheme 9 was first described by: Spencer, J. B.; Stolowich, N. J.; Roessner, C. A.; Min, C.; Scott, A. I. J. Am. Chem. Soc. 1993, 115, 11610-11611. The configuration at C-20 (tertiary alcohol) of precorrin-3x was assigned by: J. B.; Stolowich, N. J.; Wang, J.; Spencer, J. B.; Santander, P. J.; Roessner, C. A.; Scott, A. I. J. Am. Chem. Soc. 1996, 118, 1657-1662.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1657-1662
    • Stolowich, N.J.1    Wang, J.2    Spencer, J.B.3    Santander, P.J.4    Roessner, C.A.5    Scott, A.I.6
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    • Dissertation, Universität Bremen
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    • Dissertation, ETH-Zürich, Austria
    • Wehrli, P. Dissertation, ETH-Zürich, Austria, 1967.
    • (1967)
    • Wehrli, P.1


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