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Volumn 64, Issue 22, 2008, Pages 5226-5235

Synthesis of pyrimidinyl arylglycines through subsequent Mitsunobu and Petasis reactions

Author keywords

Arylglycines; Mitsunobu reaction; Nucleophilic ipso substitution; Petasis reaction; Pyrimidines; Smiles rearrangement

Indexed keywords

2 (BENZYLSULFANYL) 4(3H) PYRIMIDINONE DERIVATIVE; AMINE; AMINOALCOHOL; BENZENEBORONIC ACID; GLYCINE DERIVATIVE; GLYOXYLIC ACID; MORPHOLINE; PYRIMIDINONE DERIVATIVE; PYRIMIDINYL ARYLGLYCINE DERIVATIVE; SULFUR;

EID: 43049113547     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.03.035     Document Type: Article
Times cited : (20)

References (46)
  • 2
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    • Asymmetric synthesis of novel sterically constrained amino acids; Symposium-in-print
    • Hruby V.J., and Soloshonok V.A. (Eds)
    • Asymmetric synthesis of novel sterically constrained amino acids; Symposium-in-print. In: Hruby V.J., and Soloshonok V.A. (Eds). Tetrahedron 57 (2001) 6329
    • (2001) Tetrahedron , vol.57 , pp. 6329
  • 16
    • 0037136494 scopus 로고    scopus 로고
    • and references cited therein
    • Hang J., Li H., and Deng L. Org. Lett. 4 (2002) 3321 and references cited therein
    • (2002) Org. Lett. , vol.4 , pp. 3321
    • Hang, J.1    Li, H.2    Deng, L.3
  • 37
    • 43049146918 scopus 로고    scopus 로고
    • For recent examples of Smiles rearrangements, see:
    • For recent examples of Smiles rearrangements, see:
  • 44
    • 43049108253 scopus 로고    scopus 로고
    • note
    • Yield calculated after flash chromatography. Amine 4 was slowly turning into alcohol 5 even when stocked inside the refrigerator.
  • 45
    • 43049137881 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra of amine 4. During the dryness process amine 4 turned partially into alcohol 5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.