Kaiser, Alexander and Balbi, Miriam (1999) Chiral 1,3-diamines from a lithiated isocyanide and chiral aziridines. TETRAHEDRON-ASYMMETRY, 10 (5). pp. 1001-1014. ISSN 0957-4166,
Full text not available from this repository. (Request a copy)Abstract
Reaction of lithiated 4-methoxybenzylisocyanide with homochiral amino acid derived N-tosyl- and N-diphenylphosphinoylaziridines proceeds diastereoselectively to provide N-protected 3-isocyanoamines. Separation of the diastereomers of these adducts or the corresponding formamides, and subsequent transformations, lead to 1,3-diamines and their monoprotected and differentially bisprotected derivatives. (C) 1999 Elsevier Science Ltd. All rights reserved.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | REDUCTION; |
| Subjects: | 600 Technology > 615 Pharmacy |
| Divisions: | Chemistry and Pharmacy > Institute of Pharmacy > Pharmaceutical/Medicinal Chemistry I (Prof. Elz) |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 15 Nov 2022 07:11 |
| Last Modified: | 15 Nov 2022 07:11 |
| URI: | https://pred.uni-regensburg.de/id/eprint/48438 |
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