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Volumn 135, Issue 11, 2013, Pages 4231-4234

Enantioselective total synthesis of plectosphaeroic acid B

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVE TOTAL SYNTHESIS; NATURAL PRODUCTS; STEREO-SELECTIVE; TOTAL SYNTHESIS;

EID: 84875430466     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja401423j     Document Type: Article
Times cited : (38)

References (56)
  • 18
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    • Many ETPs possess a hydroxyl substituent adjacent to the quaternary center in the pyrrolidine ring, as found in 1 -3. Molecules of this type readily undergo fragmentation when exposed to basic or acidic conditions or triphenylphosphine, see: and references therein
    • Many ETPs possess a hydroxyl substituent adjacent to the quaternary center in the pyrrolidine ring, as found in 1-3. Molecules of this type readily undergo fragmentation when exposed to basic or acidic conditions or triphenylphosphine, see: Overman, L. E.; Shin, Y. Org. Lett. 2007, 9, 339-341 and references therein
    • (2007) Org. Lett. , vol.9 , pp. 339-341
    • Overman, L.E.1    Shin, Y.2
  • 25
    • 0042912912 scopus 로고    scopus 로고
    • For aminophenoxazinones, see ref 3 and
    • For aminophenoxazinones, see ref 3 and Estlin, E. J.; Veal, G. J. Cancer Treat. Rev. 2003, 29, 253-273
    • (2003) Cancer Treat. Rev. , vol.29 , pp. 253-273
    • Estlin, E.J.1    Veal, G.J.2
  • 29
    • 84863513722 scopus 로고    scopus 로고
    • For the total synthesis and stereochemical confirmation of (+)-gliocladin B (11), see
    • For the total synthesis and stereochemical confirmation of (+)-gliocladin B (11), see: Boyer, N.; Movassaghi, M. Chem. Sci. 2012, 3, 1798-1803
    • (2012) Chem. Sci. , vol.3 , pp. 1798-1803
    • Boyer, N.1    Movassaghi, M.2
  • 49
    • 84875419017 scopus 로고    scopus 로고
    • The relative and absolute configuration of 21a was secured by single crystal X-ray diffraction. These data have been deposited at The Cambridge Crystallographic Data Centre as entry CCDC 922842 and can be obtained free of charge via
    • The relative and absolute configuration of 21a was secured by single crystal X-ray diffraction. These data have been deposited at The Cambridge Crystallographic Data Centre as entry CCDC 922842 and can be obtained free of charge via www.ccdc.cam.ac.uk/data-request/cif.
  • 52
    • 84862930652 scopus 로고    scopus 로고
    • For recent examples of direct introduction of methylthio substituents, at the α and α′-positions of dioxopiperazines, see refs 2e, 10b, 11, 12a, 12c, and
    • For recent examples of direct introduction of methylthio substituents, at the α and α′-positions of dioxopiperazines, see refs 2e, 10b, 11, 12a, 12c, and Nicolaou, K. C.; GigueÌre, D.; Totokotsopoulos, S.; Sun, Y.-P. Angew. Chem., Int. Ed. 2012, 51, 728-732
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 728-732
    • Nicolaou, K.C.1    Gigueìre, D.2    Totokotsopoulos, S.3    Sun, Y.-P.4
  • 54
    • 79958802869 scopus 로고    scopus 로고
    • Turbomole GmbH: Karlsruhe, Germany
    • TURBOMOLE, V6.3; Turbomole GmbH: Karlsruhe, Germany, 2011; http://www.turbomole.com.
    • (2011) Turbomole, V6.3
  • 56
    • 0011822019 scopus 로고
    • See ref 5, and for the lability of aminophenoxazinones, see
    • See ref 5, and for the lability of aminophenoxazinones, see: Bolognese, A.; Piscitelli, C.; Scherillo, G. J. Org. Chem. 1983, 48, 3649-3652
    • (1983) J. Org. Chem. , vol.48 , pp. 3649-3652
    • Bolognese, A.1    Piscitelli, C.2    Scherillo, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.