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Application of allylic amine formation from aziridine-2-ol under Appel reaction condition: Synthesis of N-(tert-butoxycarbonyl)-D-vinyl glycine methyl ester
被引:1
|作者:
Chavan, Subhash P.
[1
,2
]
Kawale, Sanket A.
[1
,2
]
Patil, Niteen B.
[1
,2
]
Kalbhor, Dinesh B.
[1
,2
]
机构:
[1] CSIR NCL Natl Chem Lab, Div Organ Chem, Pune 411008, Maharashtra, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
关键词:
Aziridine-2-alcohol;
Allyl amine;
Ring opening;
Birch reaction;
Aziridinium ion;
L-ALPHA-VINYLGLYCINE;
CONVENIENT SYNTHESIS;
EFFICIENT SYNTHESIS;
ASPARTATE-AMINOTRANSFERASE;
ENANTIOSPECIFIC SYNTHESIS;
STEREOSELECTIVE-SYNTHESIS;
ASYMMETRIC-SYNTHESIS;
D-ALLITOL;
ACID;
INHIBITION;
D O I:
10.1016/j.tetlet.2021.153119
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
PPh3/I-2/imidazolde mediated allyl amine formation from aziridine-2-alcohol was explored for the synthesis of N-(tert-butoxycarbonyl)-D-vinyl glycine methyl ester. (C) 2021 Published by Elsevier Ltd.
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