메뉴 건너뛰기




Volumn 51, Issue 1, 2010, Pages 60-63

Synthesis of new β- and γ-aminopyrrolidinephosphonates via 1,3-dipolar cycloaddition of substituted vinylphosphonates

Author keywords

Aminophosphonic Acids; 1,3 Dipolar cycloaddition; Cross metathesis; Pyrrolidines; Vinylphosphonates

Indexed keywords

BETA AMINOPYRROLIDINEPHOSPHONATE DERIVATIVE; BROMINE DERIVATIVE; GAMMA AMINOPYRROLIDINEPHOSPHONATE DERIVATIVE; PHOSPHITE; PHOSPHONIC ACID DERIVATIVE; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 70649104662     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.10.087     Document Type: Article
Times cited : (34)

References (38)
  • 12
    • 17244379375 scopus 로고    scopus 로고
    • For a synthesis of β-aminophosphonates and their biological activities, see:
    • For a synthesis of β-aminophosphonates and their biological activities, see:. Palacios F., Alonso C., and de los Santos J.M. Chem. Rev. 105 (2005) 899-991
    • (2005) Chem. Rev. , vol.105 , pp. 899-991
    • Palacios, F.1    Alonso, C.2    de los Santos, J.M.3
  • 18
    • 0003592435 scopus 로고
    • For the preparation of azomethine ylide precursors and their [3+2]cycloaddition reaction with vinylsulfones, vinylcarboxylates and other dipolarophiles, see:
    • For the preparation of azomethine ylide precursors and their [3+2]cycloaddition reaction with vinylsulfones, vinylcarboxylates and other dipolarophiles, see:. Padwa A., and Dent W. Org. Synth. 67 (1988) 133-140
    • (1988) Org. Synth. , vol.67 , pp. 133-140
    • Padwa, A.1    Dent, W.2
  • 20
    • 70649097777 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon Press, Oxford
    • Padwa A. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 4 (1991), Pergamon Press, Oxford 1090-1109
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1090-1109
    • Padwa, A.1
  • 29
    • 70649090654 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 17.00.
  • 30
    • 70649085443 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 32.70.
  • 31
    • 70649102541 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 15.56.
  • 32
    • 10044226250 scopus 로고    scopus 로고
    • For a preparation of allylic phosphonates with a cross metathesis, see:
    • For a preparation of allylic phosphonates with a cross metathesis, see:. He A., Yan B., Thanaravo A., Spilling C.D., and Rath N.P. J. Org. Chem. 69 (2004) 8643-8651
    • (2004) J. Org. Chem. , vol.69 , pp. 8643-8651
    • He, A.1    Yan, B.2    Thanaravo, A.3    Spilling, C.D.4    Rath, N.P.5
  • 33
    • 70649092689 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 16.52.
  • 34
    • 70649098679 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 30.94.
  • 37
    • 70649109175 scopus 로고    scopus 로고
    • note
    • 3, 101.25 MHz) δ = 31.41.
  • 38
    • 70649095637 scopus 로고    scopus 로고
    • note
    • For other possible deprotections of amine or hydrolysis of phosphonate function, see Refs. 11,20.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.