Total synthesis of mycalamide A. Further synthetic study of the right half

Heterocycles

Volumn 42, Issue 1, 1996, Pages 159-164

  Nakata, Tadashi ^a   Fukui, Hideto ^a   Nakagawa, Tadakiyo ^a   Matsukura, Hiroko ^a  

^a INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

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EID: 0001179813     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-95-S64     Document Type: Article

References (25)

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17. Such a low selectivity or anomaly in the Sharpless asymmetric dihydroxylation was also reported by several groups: (a) ref. 5c; (b) E. M. Carreira and J. Du Bois, J. Am. Chem. Soc., 1994, 116, 10825; (c) M. Iwashita, T. Kinsho, and A. B. Smith, III, Tetrahedron Lett., 1995, 36, 2199.
18. Such a low selectivity or anomaly in the Sharpless asymmetric dihydroxylation was also reported by several groups: (a) ref. 5c; (b) E. M. Carreira and J. Du Bois, J. Am. Chem. Soc., 1994, 116, 10825; (c) M. Iwashita, T. Kinsho, and A. B. Smith, III, Tetrahedron Lett., 1995, 36, 2199.
19. Such a low selectivity or anomaly in the Sharpless asymmetric dihydroxylation was also reported by several groups: (a) ref. 5c; (b) E. M. Carreira and J. Du Bois, J. Am. Chem. Soc., 1994, 116, 10825; (c) M. Iwashita, T. Kinsho, and A. B. Smith, III, Tetrahedron Lett., 1995, 36, 2199.
20. 9
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22. In the former synthesis, 6 the overall yield of 11 from the epoxide (7) was 43% in six steps.
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