메뉴 건너뛰기




Volumn 70, Issue 44, 2014, Pages 8183-8218

Protecting group-free syntheses of natural products and biologically active compounds

Author keywords

Natural products; Organic synthesis; Protecting group free synthesis; Protecting groups

Indexed keywords

NATURAL PRODUCT; ORGANIC COMPOUND;

EID: 84921055550     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.06.025     Document Type: Review
Times cited : (49)

References (300)
  • 2
    • 0039463083 scopus 로고
    • Chemistry creates its object. This creative faculty, akin to that of art, forms an essential distinction between chemistry and the other natural or historical sciences." Mallet-Bachelier Paris
    • "Chemistry creates its object. This creative faculty, akin to that of art, forms an essential distinction between chemistry and the other natural or historical sciences." M. Berthelot Chimie Organique Fondée sur la Synthèse Vol. 2 1860 Mallet-Bachelier Paris 811
    • (1860) Chimie Organique Fondée sur la Synthèse , vol.2 , pp. 811
    • Berthelot, M.1
  • 3
    • 70350500463 scopus 로고    scopus 로고
    • A tutorial review article on the economies of synthesis
    • A tutorial review article on the economies of synthesis: T. Newhouse, P. Baran, and R.W. Hoffmann Chem. Soc. Rev. 38 2009 3010
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 3010
    • Newhouse, T.1    Baran, P.2    Hoffmann, R.W.3
  • 55
    • 34248382547 scopus 로고    scopus 로고
    • Isolation and structure elucidation
    • Isolation and structure elucidation: X.H. Cai, Z.Z. Du, and X.D. Luo Org. Lett. 9 2007 1817
    • (2007) Org. Lett. , vol.9 , pp. 1817
    • Cai, X.H.1    Du, Z.Z.2    Luo, X.D.3
  • 78
    • 84922606752 scopus 로고    scopus 로고
    • Isolation
    • Isolation
  • 92
    • 84877256728 scopus 로고    scopus 로고
    • for a recent synthesis which has only one PG-deprotection step, see
    • for a recent synthesis which has only one PG-deprotection step, see: M. Zahel, A. Kessberg, and P. Metz Angew. Chem., Int. Ed. 52 2013 5390
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 5390
    • Zahel, M.1    Kessberg, A.2    Metz, P.3
  • 106
    • 24644508752 scopus 로고    scopus 로고
    • A review article on the chemistry and biology of rhazinilam
    • A review article on the chemistry and biology of rhazinilam: O. Baudoin, D. Guenard, and F. Gueritte Mini-Rev. Org. Chem. 1 2004 333
    • (2004) Mini-Rev. Org. Chem. , vol.1 , pp. 333
    • Baudoin, O.1    Guenard, D.2    Gueritte, F.3
  • 124
    • 84922620424 scopus 로고    scopus 로고
    • The 12th issue of was dedicated to organocatalysis, with review articles by Pihko, List, Wurz, Gaunt, Enders, Maruoka, Bolm, Jacobsen, Akiyama, Colby Davie, Miller, Waymouth, Hedrick and Aggarwal
    • The 12th issue of Chem. Rev. 107 2007 was dedicated to organocatalysis, with review articles by Pihko, List, Wurz, Gaunt, Enders, Maruoka, Bolm, Jacobsen, Akiyama, Colby Davie, Miller, Waymouth, Hedrick and Aggarwal
    • (2007) Chem. Rev. , vol.107
  • 128
    • 33646558310 scopus 로고    scopus 로고
    • The eighth issue of was dedicated to organocatalysis, with review articles by List, Shi, Yang, O'Donnell, Lygo, Maruoka, Enders, Fu, Houk, Saito, Yamamoto, Barbas, Lectka, Miller, Aggarwal and Deng
    • The eighth issue of Acc. Chem. Res. 37 2004 was dedicated to organocatalysis, with review articles by List, Shi, Yang, O'Donnell, Lygo, Maruoka, Enders, Fu, Houk, Saito, Yamamoto, Barbas, Lectka, Miller, Aggarwal and Deng
    • (2004) Acc. Chem. Res. , vol.37
  • 131
    • 84922624720 scopus 로고    scopus 로고
    • Isolation
    • Isolation
  • 153
    • 84860724488 scopus 로고    scopus 로고
    • For the latest modification that uses pseudoephenamine, see
    • For the latest modification that uses pseudoephenamine, see: M.R. Morales, K.T. Mellem, and A.G. Myers Angew. Chem., Int. Ed. 51 2012 4568
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 4568
    • Morales, M.R.1    Mellem, K.T.2    Myers, A.G.3
  • 162
    • 77950790357 scopus 로고    scopus 로고
    • A review article on platensimycin and platencin
    • A review article on platensimycin and platencin: K. Palanichamy, and K.P. Kaliappan Chem.-Asian J. 5 2010 668
    • (2010) Chem.-Asian J. , vol.5 , pp. 668
    • Palanichamy, K.1    Kaliappan, K.P.2
  • 167
    • 51649100352 scopus 로고    scopus 로고
    • For a previous application of this principle in the total synthesis of platencine, see
    • For a previous application of this principle in the total synthesis of platencine, see: S.Y. Yun, J.-C. Zheng, and D. Lee Angew. Chem., Int. Ed. 47 2008 6201
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 6201
    • Yun, S.Y.1    Zheng, J.-C.2    Lee, D.3
  • 193
    • 0035143674 scopus 로고    scopus 로고
    • Isolation and structure elucidation
    • Isolation and structure elucidation: A.D. Rodriguez, and C. Ramírez J. Nat. Prod. 64 2001 100
    • (2001) J. Nat. Prod. , vol.64 , pp. 100
    • Rodriguez, A.D.1    Ramírez, C.2
  • 200
    • 0018612308 scopus 로고
    • Quinghaosu Antimalaria Coordinating Research Group Chin. Med. J 92 1979 811
    • (1979) Chin. Med. J , vol.92 , pp. 811
  • 202
    • 84897035295 scopus 로고    scopus 로고
    • A review article on syntheses of artemisinin
    • A review article on syntheses of artemisinin: S.P. Cook Synlett 2014 751
    • (2014) Synlett , pp. 751
    • Cook, S.P.1
  • 211
    • 0028882557 scopus 로고
    • the references therein
    • J. Xu, and J.-C. Yadan J. Org. Chem. 60 1995 6296 and the references therein
    • (1995) J. Org. Chem. , vol.60 , pp. 6296
    • Xu, J.1    Yadan, J.-C.2
  • 220
    • 84922608703 scopus 로고
    • in this synthesis, the rearrangement of 6,6-santonin ring system into a 5,7-system of guaianolides was not effected photochemically, but using 'classical' chemical reactions, which added 15 steps to the reaction sequence
    • M. Ando, H. Kusaka, H. Ohara, K. Takase, H. Ymaoka, and Y. Yanagi J. Org. Chem. 54 1989 1953 in this synthesis, the rearrangement of 6,6-santonin ring system into a 5,7-system of guaianolides was not effected photochemically, but using 'classical' chemical reactions, which added 15 steps to the reaction sequence
    • (1989) J. Org. Chem. , vol.54 , pp. 1953
    • Ando, M.1    Kusaka, H.2    Ohara, H.3    Takase, K.4    Ymaoka, H.5    Yanagi, Y.6
  • 228
    • 84867546407 scopus 로고    scopus 로고
    • Review article on biomimetic syntheses of flindersial alkaloids
    • Review article on biomimetic syntheses of flindersial alkaloids: R. Vallakati, and J.A. May Synlett 2012 2577
    • (2012) Synlett , pp. 2577
    • Vallakati, R.1    May, J.A.2
  • 242
    • 77749271168 scopus 로고    scopus 로고
    • A review article on taiwaniaquinones
    • A review article on taiwaniaquinones: G. Majetich, and J.M. Shimkus J. Nat. Prod. 73 2010 284
    • (2010) J. Nat. Prod. , vol.73 , pp. 284
    • Majetich, G.1    Shimkus, J.M.2
  • 249
    • 8544249232 scopus 로고
    • This type of reaction was observed earlier on irradiation of quinone with UV light
    • This type of reaction was observed earlier on irradiation of quinone with UV light: O.E. Edwards, and P.-T. Ho Can. J. Chem. 56 1978 733
    • (1978) Can. J. Chem. , vol.56 , pp. 733
    • Edwards, O.E.1    Ho, P.-T.2
  • 256
    • 70350474764 scopus 로고    scopus 로고
    • A review article on the application of enzymes in organic synthesis
    • A review article on the application of enzymes in organic synthesis: T. Hudlicky, and J.W. Reed Chem. Soc. Rev. 38 2009 3117
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 3117
    • Hudlicky, T.1    Reed, J.W.2
  • 282
    • 53849102606 scopus 로고    scopus 로고
    • Interestingly, the semipinacol rearrangement with ring contraction was also the key-step in the first synthesis of both enantiomers of peribysin E, although on a structurally different system
    • Interestingly, the semipinacol rearrangement with ring contraction was also the key-step in the first synthesis of both enantiomers of peribysin E, although on a structurally different system: A.R. Angeles, S.P. Waters, and S.J. Danishefsky J. Am. Chem. Soc. 130 2008 13765
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13765
    • Angeles, A.R.1    Waters, S.P.2    Danishefsky, S.J.3
  • 288
    • 79953061851 scopus 로고    scopus 로고
    • A review article on xanthanes and xanthanolides
    • A review article on xanthanes and xanthanolides: A. Vasas, and J. Hohmann Nat. Prod. Rep. 28 2011 824
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 824
    • Vasas, A.1    Hohmann, J.2
  • 290
    • 75849128042 scopus 로고    scopus 로고
    • A review article on dyotropic rearrangements
    • A review article on dyotropic rearrangements: I. Fernandez, F.P. Cossio, and M.A. Sierra Chem. Rev. 109 2009 6687
    • (2009) Chem. Rev. , vol.109 , pp. 6687
    • Fernandez, I.1    Cossio, F.P.2    Sierra, M.A.3
  • 295
    • 11144328091 scopus 로고    scopus 로고
    • For a review on Lycopodium alkaloids, see
    • For a review on Lycopodium alkaloids, see: X. Ma, and D.R. Gang Nat. Prod. Rep. 21 2004 752
    • (2004) Nat. Prod. Rep. , vol.21 , pp. 752
    • Ma, X.1    Gang, D.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.