Thermal decomposition mechanism and hazard assessment of di-tert-butyl azodicarboxylate (DBAD)
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s10973-023-11992-x.pdf
Reference33 articles.
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2. Mitsunobu O. The use of diethyl azodicarboxylate and triphenylphosphine in synthesis and transformation of natural products. In: Stec WJ, editor. Phosphorus chemistry directed towards biology. Pergamon: Elsevier; 1980. p. 213–8.
3. Hanrahan JR, Mewett KN, Chebib M, et al. Diastereoselective synthesis of (+/-)-(3-aminocyclopentane)alkylphosphinic acids, conformationally restricted analogues of GABA. Org Biomol Chem. 2006;4(13):2642–9. https://doi.org/10.1039/b604002k.
4. Smith AB, Safonov IG, Corbett RM. Total synthesis of (+)-zampanolide. J Am Chem Soc. 2001;49(123):12426–7. https://doi.org/10.1021/ja012220y.
5. Kang SB, Ahn EJ, Kim Y, et al. A facile synthesis of (S)-(−)-7,8-difluoro-3,4-dihydro-3-methyl-2H-1,4-benzoxazine by zinc chloride assisted mitsunobu cyclization reaction. Tetrahedron Lett. 1996;37(52):9317–20. https://doi.org/10.1016/S0040-4039(97)82952-8.
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