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Volumn 51, Issue 14, 2012, Pages 3405-3409

Total synthesis of the bacterial RNA polymerase inhibitor ripostatin B

Author keywords

antibiotics; ring closing metathesis; ripostatin; RNA polymerase; total synthesis

Indexed keywords

ALDOL REACTIONS; CARBON FRAMEWORK; HYDROXY GROUPS; RING CLOSING METATHESIS; RIPOSTATIN; RNA POLYMERASE; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; TITLE COMPOUNDS; TOTAL SYNTHESIS;

EID: 84859224183     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201200871     Document Type: Article
Times cited : (34)

References (31)
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    • Tang, W.1    Prusov, E.V.2
  • 16
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    • For a recent review on the metathesis reaction, see:, A. H. Hoveyda, A. R. Zhugralin, Nature 2007, 450, 243-251.
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    • Hoveyda, A.H.1    Zhugralin, A.R.2
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    • 13C NMR analysis of the acetonide derived from 11 by ester cleavage and acetal formation with 2,2-dimethoxypropane according to Rychnovsky et al., which proved the relative configuration of the 1,3-diol moiety to be anti:, S. D. Rychnovsky, B. N. Rogers, T. I. Richardson, Acc. Chem. Res. 1998, 31, 9-17.
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    • Rychnovsky, S.D.1    Rogers, B.N.2    Richardson, T.I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.