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Volumn 7, Issue , 2011, Pages 243-245

A two step synthesis of a key unit B precursor of cryptophycins by asymmetric hydrogenation

Author keywords

Amino acid; Asymmetric hydrogenation; Cryptophycin; DuPhos

Indexed keywords


EID: 79954522607     PISSN: 18605397     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.7.32     Document Type: Article
Times cited : (8)

References (16)
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    • (2006) Synthesis , Issue.22 , pp. 3747-3789
    • Eissler, S.1    Stoncius, A.2    Nahrwold, M.3    Sewald, N.4
  • 6
    • 33746641274 scopus 로고    scopus 로고
    • Total synthesis of cryptophycin analogues via a scaffold approach
    • DOI 10.1021/ol0609356
    • McCubbin, J. A.; Maddess, M. L.; Lautens, M. Org. Lett. 2006, 8, 2993-2996. doi:10.1021/ol0609356 (Pubitemid 44154413)
    • (2006) Organic Letters , vol.8 , Issue.14 , pp. 2993-2996
    • McCubbin, J.A.1    Maddess, M.L.2    Lautens, M.3
  • 8
    • 79954521347 scopus 로고    scopus 로고
    • Ph.D. Thesis, Bielefeld University, Bielefeld, Germany
    • Eißler, S. Synthese von Cryptophycinen für SAR-Studien. Ph.D. Thesis, Bielefeld University, Bielefeld, Germany, 2008. http://bieson.ub.uni- bielefeld.de/volltexte/2008/1301/
    • (2008) Synthese von Cryptophycinen für SAR-studien
    • Eißler, S.1
  • 12
    • 36849051865 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of α-amino acids
    • DOI 10.1021/cr050580o
    • Nájera, C.; Sansano, J. M. Chem. Rev. 2007, 107, 4584-4671. doi:10.1021/cr050580o (Pubitemid 350225862)
    • (2007) Chemical Reviews , vol.107 , Issue.11 , pp. 4584-4671
    • Najera, C.1    Sansano, J.M.2
  • 14
    • 29744453710 scopus 로고    scopus 로고
    • Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine
    • DOI 10.1039/b510761j
    • Bower, J. F.; Szeto, P.; Gallagher, T. Chem. Commun. 2005, 5793-5795. doi:10.1039/b510761j (Pubitemid 43028757)
    • (2005) Chemical Communications , Issue.46 , pp. 5793-5795
    • Bower, J.F.1    Szeto, P.2    Gallagher, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.