메뉴 건너뛰기




Volumn 19, Issue 4, 2017, Pages 878-881

Synthesis of the Tetracyclic ABCD Ring Domain of Calyciphylline A-Type Alkaloids via Reductive Radical Cyclizations

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85013168172     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.7b00035     Document Type: Article
Times cited : (31)

References (48)
  • 4
    • 2142703919 scopus 로고    scopus 로고
    • The Daphniphyllum Alkaloids
    • Cordell, G. A. Academic Press: New York
    • For a review of Heathcock's work, see: Kobayashi, J.; Morita, H. The Daphniphyllum Alkaloids. In The Alkaloids; Cordell, G. A., Eds.; Academic Press: New York; 2003; Vol. 60, pp 165-205.
    • (2003) The Alkaloids , vol.60 , pp. 165-205
    • Kobayashi, J.1    Morita, H.2
  • 5
    • 84988527661 scopus 로고    scopus 로고
    • Tantillo, D. J. Org. Lett. 2016, 18, 4482-4484 10.1021/acs.orglett.6b01919
    • (2016) Org. Lett. , vol.18 , pp. 4482-4484
    • Tantillo, D.J.1
  • 13
    • 84868368468 scopus 로고    scopus 로고
    • Yao, Y.; Liang, G. Org. Lett. 2012, 14, 5499-5501 10.1021/ol3026395
    • (2012) Org. Lett. , vol.14 , pp. 5499-5501
    • Yao, Y.1    Liang, G.2
  • 30
    • 33645790695 scopus 로고    scopus 로고
    • For the synthesis of an N-Boc analogue using a [4 + 2]-cycloaddition of 2-imido-substituted furans, see: Padwa, A.; Wang, Q. J. Org. Chem. 2006, 71, 3210-3220 10.1021/jo060238r
    • (2006) J. Org. Chem. , vol.71 , pp. 3210-3220
    • Padwa, A.1    Wang, Q.2
  • 43
    • 85013181592 scopus 로고    scopus 로고
    • CCDC 1507648 (3) contains the supplementary crystallographic data for this compound. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 44
    • 79957850855 scopus 로고    scopus 로고
    • Copper iodide acts as a phosphine scavenger, which enhances the rate of the reaction, and also as a stabilizer of the catalyst due to the iodine ion
    • Copper iodide acts as a phosphine scavenger, which enhances the rate of the reaction, and also as a stabilizer of the catalyst due to the iodine ion: Voigtritter, K.; Ghorai, S.; Lipshutz, B. H. J. Org. Chem. 2011, 76, 4697-4702 10.1021/jo200360s
    • (2011) J. Org. Chem. , vol.76 , pp. 4697-4702
    • Voigtritter, K.1    Ghorai, S.2    Lipshutz, B.H.3
  • 45
    • 84856615300 scopus 로고    scopus 로고
    • For a review of the reactivity of the Wieland-Miescher ketone as a prototype α,β-unsaturated ketone, see: Bradshaw, B.; Bonjoch, J. Synlett 2012, 23, 337-356 10.1055/s-0031-1290107
    • (2012) Synlett , vol.23 , pp. 337-356
    • Bradshaw, B.1    Bonjoch, J.2
  • 47
    • 85013182798 scopus 로고    scopus 로고
    • Ph.D. Dissertation, University of Barcelona
    • Coussanes, G. Ph.D. Dissertation, University of Barcelona, 2016.
    • (2016)
    • Coussanes, G.1
  • 48
    • 33845379788 scopus 로고
    • Enols have long been known to react avidly with oxygen to form hydroperoxy ketones, which were readily reduced, and the corresponding hydroxy ketones were isolated
    • Enols have long been known to react avidly with oxygen to form hydroperoxy ketones, which were readily reduced, and the corresponding hydroxy ketones were isolated: Zimmerman, H. E.; Linder, L. W. J. Org. Chem. 1985, 50, 1637-1646 10.1021/jo00210a016
    • (1985) J. Org. Chem. , vol.50 , pp. 1637-1646
    • Zimmerman, H.E.1    Linder, L.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.