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Volumn 9, Issue 23, 2007, Pages 4921-4923

An effective enantioselective route to the platensimycin core

Author keywords

[No Author keywords available]

Indexed keywords

ADAMANTANE; AMINOBENZOIC ACID DERIVATIVE; ANILIDE; PLATENSIMYCIN;

EID: 36348961991     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702323s     Document Type: Article
Times cited : (114)

References (19)
  • 1
    • 33744994317 scopus 로고    scopus 로고
    • Wang, J.; Soisson, S. M.; Young, K.; Shoop, W.; Kodali, S.; Galgoci, A.; Painter, R.; Parthasarathy, G.; Tang, Y. S.; Cummings, R.; Ha, S.; Dorso, K.; Motyl, M.; Jayasuriya, H.; Ondeyka, J.; Herath, K.; Zhang, C.; Hernandez, L.; Allocco, J.; Basilio, A.; Tormo, J. R.; Genilloud, O.; Vicente, F.; Pelaez, F.; Colwell, L.; Lee, S. H.; Michael, B.; Felcetto, T.; Gill, C.; Silver, L. L.; Hermes, J. D.; Bartizal, K.; Barrett, J.; Schmatz, D.; Becker, J. W.; Cully, D.; Singh, S. B. Nature 2006, 441, 358-361.
    • (a) Wang, J.; Soisson, S. M.; Young, K.; Shoop, W.; Kodali, S.; Galgoci, A.; Painter, R.; Parthasarathy, G.; Tang, Y. S.; Cummings, R.; Ha, S.; Dorso, K.; Motyl, M.; Jayasuriya, H.; Ondeyka, J.; Herath, K.; Zhang, C.; Hernandez, L.; Allocco, J.; Basilio, A.; Tormo, J. R.; Genilloud, O.; Vicente, F.; Pelaez, F.; Colwell, L.; Lee, S. H.; Michael, B.; Felcetto, T.; Gill, C.; Silver, L. L.; Hermes, J. D.; Bartizal, K.; Barrett, J.; Schmatz, D.; Becker, J. W.; Cully, D.; Singh, S. B. Nature 2006, 441, 358-361.
  • 5
    • 36348977039 scopus 로고    scopus 로고
    • Zou, Y, Chen, C-H, Taylor, C. D, Snider, B. B
    • Zou, Y.; Chen, C-H.; Taylor, C. D.; Snider, B. B.
  • 18
    • 36348966040 scopus 로고    scopus 로고
    • The required intermediate silyl enol ether was generated more selectively by trimethylamine than by other tertiary amines
    • The required intermediate silyl enol ether was generated more selectively by trimethylamine than by other tertiary amines.
  • 19
    • 33847085067 scopus 로고    scopus 로고
    • 2 syn in 1-butene. The former conformation of 1-butene is more stable than the latter by ca. 1.5 kcal/mol; see: Hemelrijk, D. V.; Enden, L. V. D.; Geise, J. J.; Sellers, H. L.; Scafer, L. J. Am. Chem. Soc. 1980, 102, 2189-2194.
    • 2 syn in 1-butene. The former conformation of 1-butene is more stable than the latter by ca. 1.5 kcal/mol; see: Hemelrijk, D. V.; Enden, L. V. D.; Geise, J. J.; Sellers, H. L.; Scafer, L. J. Am. Chem. Soc. 1980, 102, 2189-2194.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.