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Volumn 15, Issue 28, 2009, Pages 6811-6814

A new and flexible synthesis of 4-hydroxypyridines: Rapid access to caerulomycins A, e and functionalized terpyridines

Author keywords

Amides; Cyclization; Heterocycles; Natural products; Pyridines; Supramolecular chemistry

Indexed keywords

ACID CHLORIDES; ALDOL-TYPE CONDENSATION; DIKETONES; ENAMIDE; ENAMIDES; FUNCTIONALIZED; HETEROAROMATIC COMPOUNDS; HETEROCYCLES; NATURAL PRODUCTS; NEW PROTOCOL; PICOLINIC ACID; SYNTHETIC SEQUENCE; TERPYRIDINES; THIONYL CHLORIDES; THREE STAGES;

EID: 67650466821     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900939     Document Type: Article
Times cited : (50)

References (53)
  • 1
    • 2942530950 scopus 로고    scopus 로고
    • R. Chinchilla, C. Nájera, M. Yus, Chem. Rev. 2004, 104, 26672772
    • a) R. Chinchilla, C. Nájera, M. Yus, Chem. Rev. 2004, 104, 26672772
  • 4
    • 84891331475 scopus 로고    scopus 로고
    • Eds, T.J.J. Müller, U H. F. Bunz, Wiley-VCH, Weinheim
    • Functional Organic Materials (Eds.: T.J.J. Müller, U H. F. Bunz), Wiley-VCH, Weinheim, 2007.
    • (2007) Functional Organic Materials
  • 6
    • 67650490036 scopus 로고    scopus 로고
    • U S. Schubert, C. Eschbaumer, Angew. Chem. 2002, 114, 30163050;
    • b) U S. Schubert, C. Eschbaumer, Angew. Chem. 2002, 114, 30163050;
  • 7
    • 0037119317 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 2892-2926
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 2892-2926
  • 10
  • 12
    • 47549115629 scopus 로고    scopus 로고
    • for selected recent examples, see: d
    • for selected recent examples, see: d) D. Craig, F. Paina, S. C. Smith, Chem. Commun. 2008, 3408-3410;
    • (2008) Chem. Commun , pp. 3408-3410
    • Craig, D.1    Paina, F.2    Smith, S.C.3
  • 20
    • 67650481603 scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 61189268
    • a)S. Hideo, Jpn. Kokai Tokkyo Koho JP 61189268, 1986
    • (1986)
    • Hideo, S.1
  • 21
    • 67650496652 scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 54079283
    • b) M. Yasuo, Jpn. Kokai Tokkyo Koho JP 54079283, 1979.
    • (1979)
    • Yasuo, M.1
  • 22
    • 33846530457 scopus 로고    scopus 로고
    • For a review dealing with fluorinated heterocycles, see
    • For a review dealing with fluorinated heterocycles, see: M. Schlosser, Angew. Chem. 2006,118, 5558-5572;
    • (2006) Angew. Chem , vol.118 , pp. 5558-5572
    • Schlosser, M.1
  • 23
    • 67650470985 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 54325446.
    • Angew. Chem. Int. Ed. 2006, 45, 54325446.
  • 24
    • 67650475954 scopus 로고    scopus 로고
    • PCT Int. Appl. WO 2008074474
    • H.-U. Reissig, J. Dash, PCT Int. Appl. WO 2008074474, 2008
    • (2008)
    • Reissig, H.-U.1    Dash, J.2
  • 25
    • 67650487230 scopus 로고    scopus 로고
    • Ger. Offen. DE 102006059710
    • and H.-U Reissig, J. Dash, Ger. Offen. DE 102006059710, 2008.
    • (2008)
    • Reissig, H.-U.1    Dash, J.2
  • 26
    • 67650481604 scopus 로고    scopus 로고
    • The intramolecular aldol type reaction of enamides is inspired from our earlier work on alkoxyallene-based approach to pyridines, see
    • The intramolecular aldol type reaction of enamides is inspired from our earlier work on alkoxyallene-based approach to pyridines, see:
  • 32
    • 0028829479 scopus 로고
    • Enamides as starting material for pyrroles, see
    • Enamides as starting material for pyrroles, see: A. Fürstner, H. Weintritt, A. Hupperts, J. Org. Chem. 1995, 60, 6637-6641.
    • (1995) J. Org. Chem , vol.60 , pp. 6637-6641
    • Fürstner, A.1    Weintritt, H.2    Hupperts, A.3
  • 34
    • 0037019962 scopus 로고    scopus 로고
    • For the synthesis and application of fluorous pyridine derivatives, see
    • For the synthesis and application of fluorous pyridine derivatives, see: C. Rocaboy, F. Hampel, J. A. Gladysz, J. Org. Chem. 2002, 67, 6863-6870.
    • (2002) J. Org. Chem , vol.67 , pp. 6863-6870
    • Rocaboy, C.1    Hampel, F.2    Gladysz, J.A.3
  • 36
  • 38
  • 39
    • 0032543080 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 1174-1196.
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 1174-1196
  • 49
    • 38949125112 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) B. Meunier, Ace. Chem. Res. 2008, 41, 69-77
    • (2008) Ace. Chem. Res , vol.41 , pp. 69-77
    • Meunier, B.1
  • 51
    • 0141427680 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 3996-4028
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 3996-4028
  • 53
    • 67650432247 scopus 로고    scopus 로고
    • The corresponding bisnonaflate has also been prepared in 56% yield. P. Hommes, H.-U. Reissig, unpublished results.
    • The corresponding bisnonaflate has also been prepared in 56% yield. P. Hommes, H.-U. Reissig, unpublished results.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.