메뉴 건너뛰기




Volumn 51, Issue 51, 2010, Pages 6756-6759

A hetero-Diels-Alder approach to functionalized 1H-tetrazoles: Synthesis of tetrazolyl-1,2-oxazines, -oximes and 5-(1-aminoalkyl)-1H-tetrazoles

Author keywords

5 (1 Aminoalkyl) 1H tetrazoles; Cycloaddition; Nitrosovinyltetrazole; Oxazine; Oxime

Indexed keywords

1,2 OXAZINE DERIVATIVE; 1H TETRAZOLE DERIVATIVE; 5 (1 AMINOALKYL) 1H TETRAZOLE DERIVATIVE; 5 (1 NITROSOVINYL) 1 PHENYL 1H TETRAZOLE DERIVATIVE; ALKENE; ALPHA AMINO ACID; BROMOOXIME; HETEROCYCLIC COMPOUND; OXIME DERIVATIVE; TETRAZOLE DERIVATIVE; TETRAZOLYL 1,2 OXAZINE DERIVATIVE; TETRAZOLYL 1,2 OXIME DERIVATIVE; UNCLASSIFIED DRUG;

EID: 78650205574     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.10.095     Document Type: Article
Times cited : (28)

References (61)
  • 1
    • 70350506065 scopus 로고    scopus 로고
    • Reviews see: A. Lemos Molecules 14 2009 4098 4119
    • (2009) Molecules , vol.14 , pp. 4098-4119
    • Lemos, A.1
  • 3
    • 34548669268 scopus 로고    scopus 로고
    • 1-Nitrosoalkenes
    • H.U. Reissig, and R. Zimmer 1-Nitrosoalkenes G.A. Molander, Science of Synthesis Vol. 33 2006 Thieme Stuttgard, Germany 371 389
    • (2006) Science of Synthesis , vol.33 , pp. 371-389
    • Reissig, H.U.1    Zimmer, R.2
  • 20
    • 0003563365 scopus 로고    scopus 로고
    • Aminophosphinic and Aminophosphonic Acids. Chemistry and Biological Activity
    • P. Kafarski, and B. Lejczak V.P. Kukhar, H.R. Hudson, Aminophosphinic and Aminophosphonic Acids. Chemistry and Biological Activity The Biological Activity of Phosphono- and Phosphino-Peptides 2000 John Wiley & Sons Chichester 173 203 407-442
    • (2000) The Biological Activity of Phosphono- And Phosphino-Peptides , pp. 173-203
    • Kafarski, P.1    Lejczak, B.2
  • 54
    • 78650189643 scopus 로고    scopus 로고
    • note
    • 6 δ 33.7, 126.3, 129.8, 130.0, 130.3, 130.9, 135.3, 142.5, 149.8
  • 55
    • 78650216643 scopus 로고    scopus 로고
    • note
    • 3 δ 1.72-1.82 (m, 1H), 2.21-2.29 (m, 1H), 2.79-2.87 (m, 1H), 2.99-3.14 (m, 2H), 3.95-3.97 (m, 1H, 6-H), 4.01-4.12 (m, 1H, 6′-H), 5.46 (d, J = 4.8 Hz, 1H, 7a-H).
  • 61
    • 78650210359 scopus 로고    scopus 로고
    • note
    • 2 = 5.6 Hz, 1H, 1-H), 5.77 (s, 1H, 3-H of pyrrole), 6.06 (d, J = 0.8 Hz, 1H, 4-H of pyrrole), 6.62 (d, J = 0.8 Hz, 1H, 5-H of pyrrole), 7.02 (d, J = 7.6 Hz,, 2H, Ar-H), 7.47-7.57 (m, 3H, Ar-H), 8.75 (br s, 1H, N-H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.