N-tert-Butoxycarbonylaminophthalimide, a versatile reagent for the conversion of alcohols into alkylated tert-butylcarbazates or hydrazines via the Mitsunobu protocol
- 1 January 2000
- journal article
- other
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (2) , 205-207
- https://doi.org/10.1016/s0040-4039(99)02038-9
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Investigation of the Mitsunobu Reaction ofN-(2-Hydroxyethyl)-N′-Phenyl-UreasSynthetic Communications, 1999
- N-Boc ethyl oxamate: a new nitrogen nucleophile for use in Mitsunobu reactionsTetrahedron Letters, 1998
- Synthesis of N-(protected)aminophthalimides: application to the synthesis of singly labelled isoniazidJournal of the Chemical Society, Perkin Transactions 1, 1998
- Conversion of Alcohols to Protected Guanidines Using the Mitsunobu ProtocolTetrahedron Letters, 1994
- Preparation of alkyl tert-butyl iminodicarbonatesThe Journal of Organic Chemistry, 1993
- tert-Butyl [[2-(trimethylsilyl)ethyl]sulfonyl]carbamate: a new reagent for use in Mitsunobu reactionsThe Journal of Organic Chemistry, 1993
- Direct synthesis of N-protected chiral amino acids from imidodicarbonates employing either Mitsunobu or triflate alkylation. Feasibility study using lactate with particular reference to 15N-labellingJournal of the Chemical Society, Perkin Transactions 1, 1992
- Acidity of imidodicarbonates and tosylcarbamates in dimethyl sulfoxide. Correlation with yields in the Mitsunobu reactionThe Journal of Organic Chemistry, 1991
- Microbial iron chelators: total synthesis of aerobactin and its constituent amino acid, N6-acetyl-N6-hydroxylysineJournal of the American Chemical Society, 1982
- The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural ProductsSynthesis, 1981