## Abstract A modified benzyloxycarbonyl (BOC) protective group, the 3,5βdiβ__tert__βbutyl substituted BOC (3,5βtBBOC) group, was introduced to the stepwise synthesis of molecularly uniform oligourethanes based on 1,5βnaphthalene diisocyanate (NDI) and 1,4βbutanediol (BDO) for the protection of the
Synthesis and application of 3, 5-Di-tert-butylbenzyl chloroformate for the protection of amino functions and the improvement of solubility in polyurethane synthesis
β Scribed by Gunter Festel; Claus D. Eisenbach
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 213 KB
- Volume
- 341
- Category
- Article
- ISSN
- 1615-4150
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β¦ Synopsis
The benzyloxycarbonyl (BOC) group was used for the protection of amino functions in the stepwise synthesis of molecularly uniform oligourethanes based on 1,5-naphthalene diamine (NDA) as well as polyurethane (PUR) elastomers with molecularly uniform NDA-based hard segments. Whereas the poor solubility of the BOC terminated key intermediates 5 in solvents suitable for condensation reactions of oligourethane building blocks in the planned synthesis route prevented the employing of this convenient protective group, the modified 3,5-di-tert-butyl substituted BOC
π SIMILAR VOLUMES
The cyclisation of dialdehydes, obtained from sugars, with cyanoacetamide and subsequent Hofmann rearrangement is a convenient and short approach to the synthesis of 3-amino sugar derivatives branched at C-3. Thus, derivatives of 3-carbamoyL3-cyano-3-deoxy sugars l-4 were transformed into N-protecte