메뉴 건너뛰기




Volumn 73, Issue 2, 2000, Pages 409-416

Synthesis of dictyopterene A: Optically active tributylstannylcyclopropane as a chiral synthon

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; DICTYOPTERENE A; UNCLASSIFIED DRUG;

EID: 0034088935     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.73.409     Document Type: Article
Times cited : (17)

References (56)
  • 1
    • 15644378136 scopus 로고
    • A review for utilization cyclopropane in organic synthesis, see: H. N. C. Wong, M. -Y. Hon. C. -W. Tse, Y. -C. Yip, J. Tanko, and T. Hudlicky, Chem. Rev., 89, 165 (1989). For recent examples, see: A. G. M. Barrett and W. Tam, J. Org. Chem., 62, 4653 and 7673 (1997), and references cited therein.
    • (1989) Chem. Rev. , vol.89 , pp. 165
    • Wong, H.N.C.1    Hon, M.-Y.2    Tse, C.-W.3    Yip, Y.-C.4    Tanko, J.5    Hudlicky, T.6
  • 2
    • 0000985430 scopus 로고    scopus 로고
    • and references cited therein
    • A review for utilization cyclopropane in organic synthesis, see: H. N. C. Wong, M. -Y. Hon. C. -W. Tse, Y. -C. Yip, J. Tanko, and T. Hudlicky, Chem. Rev., 89, 165 (1989). For recent examples, see: A. G. M. Barrett and W. Tam, J. Org. Chem., 62, 4653 and 7673 (1997), and references cited therein.
    • (1997) J. Org. Chem. , vol.62 , pp. 4653
    • Barrett, A.G.M.1    Tam, W.2
  • 6
    • 84981962866 scopus 로고
    • d) L. Jaenicke and W. Boland, Angew. Chem., Int. Ed. Engl., 21, 643 (1982). Absolute configuration of dictyopterene A was wrong registered as (1R,2R) in these references. This should be corrected to (1S,2R); M. Hombeck, G. Pohnert, and W. Boland, Chem. Commun., 1999, 243.
    • (1982) Angew. Chem., Int. Ed. Engl. , vol.21 , pp. 643
    • Jaenicke, L.1    Boland, W.2
  • 7
    • 0033531377 scopus 로고    scopus 로고
    • d) L. Jaenicke and W. Boland, Angew. Chem., Int. Ed. Engl., 21, 643 (1982). Absolute configuration of dictyopterene A was wrong registered as (1R,2R) in these references. This should be corrected to (1S,2R); M. Hombeck, G. Pohnert, and W. Boland, Chem. Commun., 1999, 243.
    • Chem. Commun. , vol.1999 , pp. 243
    • Hombeck, M.1    Pohnert, G.2    Boland, W.3
  • 8
    • 0026021948 scopus 로고
    • Because of its unique biological activity, several syntheses of this compound have been reported. a) D. Grandjean, P. Pale, and J. Chuche, Tetrahedron, 47, 1215 (1991).
    • (1991) Tetrahedron , vol.47 , pp. 1215
    • Grandjean, D.1    Pale, P.2    Chuche, J.3
  • 13
    • 0039424187 scopus 로고    scopus 로고
    • Several synthesis of optically active (4a) has been reported. a) Y. Ukaji, K. Sada, and K. Inomata, Chem. Lett., 1993, 1227.
    • Chem. Lett. , vol.1993 , pp. 1227
    • Ukaji, Y.1    Sada, K.2    Inomata, K.3
  • 25
    • 0001728270 scopus 로고    scopus 로고
    • A. B. Charette and H. Juteau, J. Am. Chem. Soc., 116, 2651 (1994). For review see: A. B. Charette and J. -F. Marcoux, Synlett, 1996, 1197.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2651
    • Charette, A.B.1    Juteau, H.2
  • 26
    • 0001728270 scopus 로고    scopus 로고
    • A. B. Charette and H. Juteau, J. Am. Chem. Soc., 116, 2651 (1994). For review see: A. B. Charette and J. -F. Marcoux, Synlett, 1996, 1197.
    • Synlett , vol.1996 , pp. 1197
    • Charette, A.B.1    Marcoux, J.-F.2
  • 50
    • 84943950090 scopus 로고
    • A review see: A. Suzuki, Pure Appl. Chem., 63, 419 (1991). For our employed reaction conditions see: I. D. Gridnev, N. Miyaura, and A. Suzuki, J. Org. Chem., 58, 5351 (1993).
    • (1991) Pure Appl. Chem. , vol.63 , pp. 419
    • Suzuki, A.1
  • 51
    • 33751386087 scopus 로고
    • A review see: A. Suzuki, Pure Appl. Chem., 63, 419 (1991). For our employed reaction conditions see: I. D. Gridnev, N. Miyaura, and A. Suzuki, J. Org. Chem., 58, 5351 (1993).
    • (1993) J. Org. Chem. , vol.58 , pp. 5351
    • Gridnev, I.D.1    Miyaura, N.2    Suzuki, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.