메뉴 건너뛰기




Volumn 1991, Issue 4, 1991, Pages 375-379

Preparation and use of chloromethyl (−)‐menthyl ether in the synthesis of optically pure α‐branched α‐amino nitriles

Author keywords

Chiral chloromethyl ethers; Pipecolic acid, 2 methyl; Proline, methyl

Indexed keywords


EID: 84986678846     PISSN: 01702041     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/jlac.199119910165     Document Type: Article
Times cited : (17)

References (18)
  • 6
    • 84986723550 scopus 로고    scopus 로고
    • 1H‐NMR spectrum. Since these resonances are characteristic they are used for the determination of the distribution of 3a and 3b in their mixtures.
  • 7
    • 84986696357 scopus 로고    scopus 로고
    • (6b) – The ratio of 1a to 1b was determined by 1H‐NMR spectrometry as 1:1 after derivatization of the mixture with 2a.
  • 8
    • 3643118353 scopus 로고
    • Asymmetrische Synthese cyclischer α-Aminosäuren nach der Bislactimether-Methode
    • α‐Methylproline and its higher cyclic analogs were prepared by Schöllkopf and co‐workers according to the bislactim ether method
    • (1987) Angewandte Chemie , vol.99 , pp. 137
    • Schöllkopf, U.1    Hinrichs, R.2    Lonsky, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.