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Volumn 3, Issue 9, 2001, Pages 1261-1263

Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; BIOLOGICAL PRODUCT; DIAZONAMIDE A; FUSED HETEROCYCLIC RINGS; OXAZOLE DERIVATIVE; POLYMER;

EID: 0035799896     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0157196     Document Type: Article
Times cited : (68)

References (34)
  • 5
    • 0042621821 scopus 로고    scopus 로고
    • Ph.D. Dissertation, Harvard University, Cambridge, MA
    • (d) Jamison, T. F. Ph.D. Dissertation, Harvard University, Cambridge, MA, 1997.
    • (1997)
    • Jamison, T.F.1
  • 26
    • 0000584326 scopus 로고
    • 2SiLi to benzaldehyde followed by acylation, while the TMS and TBS derivatives were prepared by a retro-Brook rearrangement (Linderman, R. J.; Ghannam, A. J. Am. Chem. Soc. 1990, 112, 2392-2398) on the α-tributylstannyl silyl-protected benzyl alcohol followed by acylation.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2392-2398
    • Linderman, R.J.1    Ghannam, A.2
  • 28
    • 0042621766 scopus 로고    scopus 로고
    • note
    • A 1:1 mixture of stereoisomers was obtained.
  • 30
    • 0043122616 scopus 로고    scopus 로고
    • note
    • Calculations (6-31G*) suggest little ground-state energy preference for the s-trans conformation over the s-cis (1.4 kcal/mol) for the imide. In the case of the ester, this preference is considerable (> 16 kcal/mol). (equation presented)
  • 34
    • 0010640653 scopus 로고
    • Determined by analysis of the Mosher amide derivatives of 22 with both (R)- and (S)-MTPA. Dale, J. A.; Dull, D. L.; Mosher, H. S. J. Org. Chem. 1969, 34, 2543-2549.
    • (1969) J. Org. Chem. , vol.34 , pp. 2543-2549
    • Dale, J.A.1    Dull, D.L.2    Mosher, H.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.