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Volumn 13, Issue 13, 2011, Pages 3360-3363

Synthesis and structural revision of phomopsin B, a novel polyketide carrying a 10-membered cyclic-ether ring

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; ETHER DERIVATIVE; PHENYLACETIC ACID DERIVATIVE;

EID: 79959739564     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2011117     Document Type: Article
Times cited : (17)

References (36)
  • 3
    • 0000921499 scopus 로고
    • Shipchandler, M. T., and references cited therein
    • Shipchandler, M. T. Heterocycles 1975, 3, 471-520 and references cited therein
    • (1975) Heterocycles , vol.3 , pp. 471-520
  • 11
    • 79959769864 scopus 로고    scopus 로고
    • 2 elimination as a side product. See
    • 2 elimination as a side product. See
  • 15
    • 0000927905 scopus 로고    scopus 로고
    • Synthesis of (±)-helianane with a 8-membered ring via olefin metathesis was reported. See: Stefinovic, M.; Snieckus, V.
    • Synthesis of (±)-helianane with a 8-membered ring via olefin metathesis was reported. See: Stefinovic, M.; Snieckus, V. J. Org. Chem. 1998, 63, 2808-2809
    • (1998) J. Org. Chem. , vol.63 , pp. 2808-2809
  • 21
    • 79959748611 scopus 로고    scopus 로고
    • 3. (11)
    • 3. (11)
  • 23
    • 79959750967 scopus 로고    scopus 로고
    • For the structures of open-chain and cyclic dimers and their structural determination, see Supporting Information.
    • For the structures of open-chain and cyclic dimers and their structural determination, see Supporting Information.
  • 24
    • 79959767465 scopus 로고    scopus 로고
    • Grubbs-Hoveyda catalysts first and second generation were also employed for the metathesis. However, the desired product was obtained in a low yield (4-10%).
    • Grubbs-Hoveyda catalysts first and second generation were also employed for the metathesis. However, the desired product was obtained in a low yield (4-10%).
  • 25
    • 79959757287 scopus 로고    scopus 로고
    • See Supporting Information.
    • See Supporting Information.
  • 27
    • 79959715018 scopus 로고    scopus 로고
    • D value was denoted.
    • D value was denoted.
  • 28
    • 79959752328 scopus 로고    scopus 로고
    • Its absolute configuration is not shown.
    • Its absolute configuration is not shown.
  • 32
    • 79959736923 scopus 로고    scopus 로고
    • 6 are summarized in Tables 2S and 3S; see Supporting Information.
    • 6 are summarized in Tables 2S and 3S; see Supporting Information.
  • 33
    • 79959722989 scopus 로고    scopus 로고
    • D of both natural products was reported to be negative although there was a discrepancy with their magnitude between refs 1 and 19.
    • D of both natural products was reported to be negative although there was a discrepancy with their magnitude between refs 1 and 19.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.