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Volumn 128, Issue 37, 2006, Pages 12050-12051

Gold-catalyzed 1,2-migration of silicon, tin, and germanium en route to C-2 substituted fused pyrrole-containing heterocycles

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; CARBON; DEUTERIUM; GERMANIUM; GOLD; HETEROCYCLIC NITRO COMPOUND; INDOLIZINE DERIVATIVE; NITROGEN; PYRIDINE DERIVATIVE; PYRROLE DERIVATIVE; SILICON; TIN; TOLUENE;

EID: 33748774952     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja063278l     Document Type: Article
Times cited : (273)

References (38)
  • 12
    • 33748763533 scopus 로고    scopus 로고
    • note
    • See Supporting Information for details.
  • 13
    • 33748783027 scopus 로고    scopus 로고
    • note
    • 9
  • 29
  • 30
    • 33748795776 scopus 로고    scopus 로고
    • note
    • For Au-catalyzed propargyl-allenyl prototropic isomerization, see ref 11c.
  • 35
    • 33748796854 scopus 로고    scopus 로고
    • note
    • 3 as a precatalyst, the latter can be reduced to Au(I) species via various redox processes. See ref 11b for discussion.
  • 37
    • 33748788763 scopus 로고    scopus 로고
    • note
    • 9 For deuterium scrambling in N-unsubstituted pyrrole ring in the presence of Au(I) complexes, see ref 11h.
  • 38
    • 33748768172 scopus 로고    scopus 로고
    • note
    • Equal distribution of deuterium between positions C-2 and C-3 is possible via path A if there is no H/D kinetic isotope effect (transformation 6 to 4). Obviously, path B cannot explain the observed scrambling of deuterium at C-2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.