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Volumn 62, Issue 39, 2006, Pages 9268-9279

A synthesis of optically active α-quaternary α-amino acids and esters by assembling three components, ketones, (R)-chloromethyl p-tolyl sulfoxide, and sodium azide, via sulfinyloxiranes

Author keywords

Amino acid; Quaternary amino acid; Asymmetric synthesis; Cyclic amino acid; Sulfinyloxirane

Indexed keywords

2 AMINOALDEHYDE; ALDEHYDE; ALKANE; ALPHA AMINO ACID; ALPHA AZIDO ALDEHYDE; BENZYLAMINE; CHLOROMETHYL 4 TOLYL SULFOXIDE; ESTER; ESTER DERIVATIVE; IODINE; KETONE; LITHIUM; LITHIUM ALPHA SULFINYL CARBANION; METHANOL; POTASSIUM HYDROXIDE; SODIUM AZIDE; SODIUM CHLORITE; SULFINYLOXIRANE; SULFOXIDE; UNCLASSIFIED DRUG;

EID: 33747004619     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.06.112     Document Type: Article
Times cited : (16)

References (53)
  • 9
    • 33747003483 scopus 로고    scopus 로고
    • Some recent reviews and papers concerning α-quaternary α-amino acids:
  • 19
    • 33746971673 scopus 로고    scopus 로고
    • Some recent reviews and papers concerning cyclic α-quaternary α-amino acids:
  • 40
    • 15244355590 scopus 로고    scopus 로고
    • Preliminary results of this study were reported as a communication
    • Preliminary results of this study were reported as a communication. Satoh T., Hirano M., and Kuroiwa A. Tetrahedron Lett. 46 (2005) 2659
    • (2005) Tetrahedron Lett. , vol.46 , pp. 2659
    • Satoh, T.1    Hirano, M.2    Kuroiwa, A.3
  • 50
    • 33747013088 scopus 로고    scopus 로고
    • note
    • One equivalent of (R)-chloromethyl p-tolyl sulfoxide was reacted with 1.4 equiv of β-tetralone. The yield was calculated based on the sulfoxide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.