Hi everyone,
What options do we have for deprotection of allyl amine besides palladium catalyst?
Thank you
DDQ - http://www.sciencedirect.com/science/article/pii/S0040403914018541
Grubbs carbene (Ru based) - http://pubs.acs.org/doi/abs/10.1021/ol0167412
http://onlinelibrary.wiley.com/doi/10.1002/chem.200305236/abstract
i agree with Eugene Yang
deprotected to give polyglycerol, using palladium over charcoal methods
http://www.organic-chemistry.org/abstracts/literature/764.shtm
http://pubs.acs.org/doi/abs/10.1021/ol016278t?journalCode=orlef7
http://www.sciencedirect.com/science/article/pii/S0040402097009204
http://onlinelibrary.wiley.com/doi/10.1002/ejoc.200500204/abstract
Thank you very much for your answers.
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