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Volumn 37, Issue 20, 1998, Pages 2883-2886

Metalated 2-alkenylsulfoximides in asymmetric synthesis: Diastereoselective preparation of highly substituted pyrrolidine derivatives

Author keywords

Asymmetric synthesis; Heterocycles; Pyrrolidines; Samarium; Sulfoximines

Indexed keywords

DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; GLYCOSIDASE INHIBITOR; PYRROLIDINE DERIVATIVE;

EID: 0032476786     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19981102)37:20<2883::AID-ANIE2883>3.0.CO;2-Y     Document Type: Article
Times cited : (45)

References (42)
  • 8
    • 0000693487 scopus 로고
    • (Ed.: Atta-Ur-Rahman), Elsevier, Amsterdam
    • W. H. Pearson in Studies in Natural Product Chemistry, Vol. 1 (Ed.: Atta-Ur-Rahman), Elsevier, Amsterdam, 1988, pp. 323-358.
    • (1988) Studies in Natural Product Chemistry , vol.1 , pp. 323-358
    • Pearson, W.H.1
  • 12
    • 0025085749 scopus 로고
    • and references therein
    • Angew. Chem. Int. Ed. Engl. 1990, 29, 1169-1171, and references therein.
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 1169-1171
  • 33
    • 33646102246 scopus 로고    scopus 로고
    • unpublished results
    • 1H NMR signal of the aldehyde protons: M. Reggelin, T. Heinrich, unpublished results.
    • Reggelin, M.1    Heinrich, T.2
  • 34
    • 33847529510 scopus 로고    scopus 로고
    • Raney Nickel requires a large excess (> 10 equiv) to provide satisfying results, and much of the pyrrolidine formed is absorbed. Lithium naphthalenide works fast, but ring-opened by-products are formed
    • Raney Nickel requires a large excess (> 10 equiv) to provide satisfying results, and much of the pyrrolidine formed is absorbed. Lithium naphthalenide works fast, but ring-opened by-products are formed.
  • 35
    • 33847525857 scopus 로고    scopus 로고
    • Desilyation of the TMS-protected derivative occurs by solvolysis during the desulfuration. More stable silyl ethers must be previously cleaved in an extra step
    • Desilyation of the TMS-protected derivative occurs by solvolysis during the desulfuration. More stable silyl ethers must be previously cleaved in an extra step.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.