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Volumn , Issue 8, 2006, Pages 1272-1274

Highly diastereoselective synthesis of N-tert-butylsulfinylpropargylamines through direct addition of alkynes to N-tert-butanesulfinimines

Author keywords

Alkynylation; Diastereoselectivity; Imine; N tert butylsulfinylpropargylamine

Indexed keywords

ALKYNE DERIVATIVE; AMINE; IMINE; N TERT BUTYLSULFINIMINE DERIVATIVE; N TERT BUTYLSULFINYLPROPARGYLAMINE DERIVATIVE; PHENYLACETYLENE; UNCLASSIFIED DRUG;

EID: 33744491803     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939076     Document Type: Article
Times cited : (47)

References (55)
  • 30
    • 4143050401 scopus 로고    scopus 로고
    • (b) For a review on reaction of p-toluenesulfinyl imines, see: Zhou, P.; Chen, B.-C.; Davis, F. A. Tetrahedron 2004, 60, 8003.
    • (2004) Tetrahedron , vol.60 , pp. 8003
    • Zhou, P.1    Chen, B.-C.2    Davis, F.A.3
  • 46
    • 33744484026 scopus 로고    scopus 로고
    • note
    • X-ray analysis of products 3aa showed that main product has anti-configuration.
  • 47
    • 33744471407 scopus 로고    scopus 로고
    • note
    • 25NOS: C, 70.06; H, 8.65; N, 4.81. Found: C, 69.94; H, 8.66; N: 4.54.
  • 49
    • 0042096802 scopus 로고
    • Patai, S.; Rappoport, Z., Eds.; Wiley: New York
    • (b) Simandi, L. I. In The Chemistry of Functional Groups; Patai, S.; Rappoport, Z., Eds.; Wiley: New York, 1983, Suppl. C, Part 1, 529-534.
    • (1983) The Chemistry of Functional Groups , Issue.SUPPL. C AND PART 1 , pp. 529-534
    • Simandi, L.I.1
  • 55
    • 33744468800 scopus 로고    scopus 로고
    • note
    • A product with 96% de was obtained when optically active 1a and 2a were used as substrates.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.