A catalyst-free 1,4-Michael-type reaction of in situ generated ortho-quinone methides (o-QMs) with dithiocarbamic acid salts in water
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s13738-019-01644-z.pdf
Reference45 articles.
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3. M.S. Singh, A. Nagaraju, N. Ananda, S. Chowdhury, ortho-Quinone methide (o-QM): a highly reactive, ephemeral and versatile intermediate in organic synthesis. RSC Adv. 4, 55924–55959 (2014)
4. P. Wan, B. Barker, L. Diao, M. Fischer, Y. Shi, C. Yang, Quinone methides: relevant intermediates in organic chemistry. Can. J. Chem. 74, 465–475 (1996)
5. J.P. Richard, M.M. Toteva, J. Crugeiras, Structure–reactivity relationships and intrinsic reaction barriers for nucleophile additions to a quinone methide: a strongly resonance-stabilized carbocation. J. Am. Chem. Soc. 122, 1664–1674 (2000)
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