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Volumn 75, Issue 1, 2010, Pages 57-68

Perylenequinone natural products: Total synthesis of hypocrellin A

Author keywords

[No Author keywords available]

Indexed keywords

2-NAPHTHOLS; AXIAL CHIRALITY; CHEMICAL EQUATIONS; CHIRAL INTERMEDIATES; DIKETONES; ENANTIOSELECTIVE; HYPOCRELLIN A; IODOBENZENE; KEY FEATURE; NATURAL PRODUCTS; SEVEN-MEMBERED RINGS; STEREO-SELECTIVE; TOTAL SYNTHESIS;

EID: 73449089773     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901386d     Document Type: Article
Times cited : (61)

References (44)
  • 3
    • 73449099486 scopus 로고    scopus 로고
    • 2-symmetric due to the same identity of the C7,C7′-positions.
    • 2-symmetric due to the same identity of the C7,C7′-positions.
  • 5
    • 0001297737 scopus 로고
    • hypocrellin A is called shiraiachrome B here
    • Wu, H; Lao, X. F.; Wang, Q. W.; Lu, R. R. J. Nat. Prod. 1989, 52, 948-951. (hypocrellin A is called shiraiachrome B here).
    • (1989) J. Nat. Prod , vol.52 , pp. 948-951
    • Wu, H.1    Lao, X.F.2    Wang, Q.W.3    Lu, R.R.4
  • 7
    • 73449127104 scopus 로고    scopus 로고
    • SciFinder indexes hypocrellin and hypocrellin A as the identical compound
    • SciFinder indexes hypocrellin and hypocrellin A as the identical compound.
  • 21
    • 33747448023 scopus 로고    scopus 로고
    • For selected examples, see: a
    • For selected examples, see: (a) Miyahara, Y. J. Org. Chem. 2006, 71, 6516-6521.
    • (2006) J. Org. Chem , vol.71 , pp. 6516-6521
    • Miyahara, Y.1
  • 34
    • 23744473269 scopus 로고    scopus 로고
    • For a simple synthetic approach to allylated aromatics via the Suzuki-Miyaura cross-coupling reaction, see: Kotha, S, Behera, M, Shah, V. Synlett 2005, 1877-1880
    • For a simple synthetic approach to allylated aromatics via the Suzuki-Miyaura cross-coupling reaction, see: Kotha, S.; Behera, M.; Shah, V. Synlett 2005, 1877-1880.
  • 35
    • 73449143706 scopus 로고    scopus 로고
    • See ref 9a for another report of a dihydroperylenequinone
    • See ref 9a for another report of a dihydroperylenequinone.
  • 36
    • 0001353830 scopus 로고    scopus 로고
    • 2 as a catalyst for deacetalization, see: Lipshutz, B. H.; Pollart, D.; Monforte, J.; Kotsuki, H. Tetrahedron Lett. 1985, 26, 705-708.
    • 2 as a catalyst for deacetalization, see: Lipshutz, B. H.; Pollart, D.; Monforte, J.; Kotsuki, H. Tetrahedron Lett. 1985, 26, 705-708.
  • 37
    • 0030038521 scopus 로고    scopus 로고
    • Protic acid protocol: Horper, W.; Marner, F.-J. Phytochemistry 1996, 41, 451.
    • Protic acid protocol: Horper, W.; Marner, F.-J. Phytochemistry 1996, 41, 451.
  • 38
    • 0000928370 scopus 로고    scopus 로고
    • Copper/quinoline protocol: Cohen, T.; Schambach, R. A. J. Am. Chem. Soc. 1970, 92, 3189.
    • Copper/quinoline protocol: Cohen, T.; Schambach, R. A. J. Am. Chem. Soc. 1970, 92, 3189.
  • 40
    • 85077854948 scopus 로고
    • For synthetic applications of NaCN in dealkoxycarbonylations, see: a
    • For synthetic applications of NaCN in dealkoxycarbonylations, see: (a) Krapcho, A. P. Synthesis 1982, 805-822.
    • (1982) Synthesis , pp. 805-822
    • Krapcho, A.P.1
  • 42
    • 73449112501 scopus 로고    scopus 로고
    • Still, W. C. MacroModel, V4.0, V5.0, V6.0, V6.5; Columbia University.
    • Still, W. C. MacroModel, V4.0, V5.0, V6.0, V6.5; Columbia University.
  • 44
    • 73449124297 scopus 로고    scopus 로고
    • See theexperimental description in the second paper of this series (DOI: 10.1021/jo901384h).
    • See theexperimental description in the second paper of this series (DOI: 10.1021/jo901384h).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.