메뉴 건너뛰기




Volumn 54, Issue 6, 2015, Pages 1933-1936

Total synthesis of the protected aglycon of fidaxomicin (tiacumicin B, lipiarmycin A3)

Author keywords

Antibiotics ; Cross coupling ; Natural products ; Stereoselective synthesis

Indexed keywords

ANTIBIOTICS; BIOACTIVITY; CHEMICAL REACTIONS; CONDENSATION REACTIONS; KETONES; STEREOCHEMISTRY; STEREOSELECTIVITY;

EID: 84922042081     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201409464     Document Type: Article
Times cited : (55)

References (73)
  • 4
    • 84870882261 scopus 로고    scopus 로고
    • An excellent review on the chemistry and biology of tiacumicin since their discovery
    • An excellent review on the chemistry and biology of tiacumicin since their discovery: W. Erb, J. Zhu, Nat. Prod. Rep. 2013, 30, 161-174
    • (2013) Nat. Prod. Rep. , vol.30 , pp. 161-174
    • Erb, W.1    Zhu, J.2
  • 11
    • 84922042675 scopus 로고    scopus 로고
    • Erb W.,Thesis Ph.D. University of Paris-Sud XI, France
    • W. Erb, Ph.D. Thesis, University of Paris-Sud XI, France, 2010.
    • (2010)
  • 12
    • 0020485245 scopus 로고
    • Previous synthesis of 2-O-methyl-d -rhamnose
    • Previous synthesis of 2-O-methyl-d -rhamnose: a) A. Lipták, Carbohydr. Res. 1982, 107, 300-302
    • (1982) Carbohydr. Res. , vol.107 , pp. 300-302
    • Lipták, A.1
  • 14
    • 0022653185 scopus 로고
    • Previous synthetic studies on noviose
    • Previous synthetic studies on noviose: a) A. Klemer, M. Waldmann, Liebigs Ann. Chem. 1986, 2, 221-225
    • (1986) Liebigs Ann. Chem. , vol.2 , pp. 221-225
    • Klemer, A.1    Waldmann, M.2
  • 15
    • 84922042674 scopus 로고
    • (Merck & Co), US
    • b) E. Walton (Merck & Co), US 2938900, 1960.
    • (1960)
    • Walton, E.1
  • 16
    • 84986727491 scopus 로고
    • Previous synthesis of resorcylic acid
    • Previous synthesis of resorcylic acid: a) M. Alexy, H.-D. Scharf, Liebigs Ann. Chem. 1991, 1363-1364.
    • (1991) Liebigs Ann. Chem. , pp. 1363-1364
    • Alexy, M.1    Scharf, H.-D.2
  • 24
    • 10044286175 scopus 로고    scopus 로고
    • for applications of this methodology to the synthesis of natural products, see
    • for applications of this methodology to the synthesis of natural products, see: b) S. Hosokawa, T. Ogura, H. Togashi, K. Tatsuta, Tetrahedron Lett. 2005, 46, 333-337
    • (2005) Tetrahedron Lett. , vol.46 , pp. 333-337
    • Hosokawa, S.1    Ogura, T.2    Togashi, H.3    Tatsuta, K.4
  • 33
    • 84896135761 scopus 로고    scopus 로고
    • for a recent review on VMAR in natural product synthesis, see
    • for a recent review on VMAR in natural product synthesis, see: M. Kalesse, M. Cordes, G. Symkenberg, H.-H. Lu, Nat. Prod. Rep. 2014, 31, 563-594.
    • (2014) Nat. Prod. Rep. , vol.31 , pp. 563-594
    • Kalesse, M.1    Cordes, M.2    Symkenberg, G.3    Lu, H.-H.4
  • 34
    • 79952153980 scopus 로고    scopus 로고
    • An example of Mitsunobu reaction carried out on a similar substrate
    • An example of Mitsunobu reaction carried out on a similar substrate: K. Kobayashi, Y. Fujii, I. Hayakawa, H. Kigoshi, Org. Lett. 2011, 13, 900-903.
    • (2011) Org. Lett. , vol.13 , pp. 900-903
    • Kobayashi, K.1    Fujii, Y.2    Hayakawa, I.3    Kigoshi, H.4
  • 49
    • 20444482463 scopus 로고    scopus 로고
    • Examples of similar epoxide opening reactions
    • Examples of similar epoxide opening reactions: a) K. C. O'Brien, E. A. Colby, T. F. Jamison, Tetrahedron 2005, 61, 6243-6248
    • (2005) Tetrahedron , vol.61 , pp. 6243-6248
    • O'Brien, K.C.1    Colby, E.A.2    Jamison, T.F.3
  • 67
    • 84922042672 scopus 로고    scopus 로고
    • Yamaguchi esterification (Eds.: J. J. Li, E. J. Corey), Wiley, Hoboken, NJ
    • "Yamaguchi esterification": N. M. Ahmad in Name Reactions for Functional Group Transformations (Eds.: J. J. Li, E. J. Corey), Wiley, Hoboken, NJ, 2007, pp. 545-550.
    • (2007) N. M. Ahmad in Name Reactions for Functional Group Transformations , pp. 545-550
  • 68
    • 22744448499 scopus 로고    scopus 로고
    • A review of applications of RCM for macrocyclization in natural product synthesis
    • A review of applications of RCM for macrocyclization in natural product synthesis: a) K. C. Nicolaou, P. G. Bulger, D. Sarlah, Angew. Chem. Int. Ed. 2005, 44, 4490-4527
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4490-4527
    • Nicolaou, K.C.1    Bulger, P.G.2    Sarlah, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.