메뉴 건너뛰기




Volumn 77, Issue 20, 2012, Pages 9304-9312

Mechanistic insight into the formation of tetraarylazadipyrromethenes

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL SOLVENT; GAIN INSIGHT; NMR ANALYSIS; PYRROLE RING; REACTION CONDITIONS; REACTION PATHWAYS; REACTION SEQUENCES; RING OPENING; SYNTHETIC ROUTES;

EID: 84867730043     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301972w     Document Type: Article
Times cited : (45)

References (48)
  • 3
  • 32
    • 33947313461 scopus 로고
    • For example, see dehydration of p -hydroxyphenylhydroxylamine
    • For example, see dehydration of p -hydroxyphenylhydroxylamine: Blount, H. N.; Herman, H. B. J. Phys. Chem. 1968, 72, 3006-3012
    • (1968) J. Phys. Chem. , vol.72 , pp. 3006-3012
    • Blount, H.N.1    Herman, H.B.2
  • 38
    • 33645791590 scopus 로고    scopus 로고
    • The chemical shift value obtained for the pyrrole nitrogen is comparable to that obtained for the pyrrole nitrogen in meso -(phenyl)dipyrromethene at -156.2 ppm
    • The chemical shift value obtained for the pyrrole nitrogen is comparable to that obtained for the pyrrole nitrogen in meso -(phenyl)dipyrromethene at -156.2 ppm: Wood, T. E.; Berno, B.; Beshara, C. S.; Thompson, A. J. Org. Chem. 2006, 71, 2964-2971
    • (2006) J. Org. Chem. , vol.71 , pp. 2964-2971
    • Wood, T.E.1    Berno, B.2    Beshara, C.S.3    Thompson, A.4
  • 48
    • 37049042297 scopus 로고
    • An analogous rearrangement would be the Dimroth rearrangement; see
    • An analogous rearrangement would be the Dimroth rearrangement; see Perrin, D. D.; Pitman, I. H. J. Chem. Soc. 1965, 7071-7082
    • (1965) J. Chem. Soc. , pp. 7071-7082
    • Perrin, D.D.1    Pitman, I.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.