tag:blogger.com,1999:blog-5299119331285745392.post6166793878172438822..comments2023-09-27T03:47:09.791-07:00Comments on Organosynthetic & Organometallic Chemistry: deprotection of benzyl methyl ether.Weiwei TIANhttp://www.blogger.com/profile/05355339462714688547noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-5299119331285745392.post-31769598381800202872018-08-30T12:28:09.127-07:002018-08-30T12:28:09.127-07:00Alfa Chemistry employs more than 200 full time sta...Alfa Chemistry employs more than 200 full time staff, of which approximate 80 are Ph.D. and M.S. chemists, specialized in synthetic chemistry, process optimization, and research. <a href="http://www.alfa-chemistry.com/cas_41381-97-9.htm" rel="nofollow">benzoylacetic acid</a><br />alfachemistryhttps://www.blogger.com/profile/05704541170361426886noreply@blogger.comtag:blogger.com,1999:blog-5299119331285745392.post-25365682684037614452008-06-20T10:04:00.000-07:002008-06-20T10:04:00.000-07:00If you can, oxidize the benzyl to benzoyl ester, t...If you can, oxidize the benzyl to benzoyl ester, then hydrolyze it.<BR/>RuO2/NaIO4.Weiwei TIANhttps://www.blogger.com/profile/05355339462714688547noreply@blogger.comtag:blogger.com,1999:blog-5299119331285745392.post-2122990210671148082008-06-20T05:31:00.000-07:002008-06-20T05:31:00.000-07:00i have synthesized a mannose anchored quaternary a...i have synthesized a mannose anchored quaternary ammonium salt with two long alkyl chains for my work. this mannose is protected with benzyl ether (4 -OBn except anomeric position). can u suggest me which would be better deprotecting agent for my compound other than catalytic hydrogenation or avoiding acetic acid.Anonymousnoreply@blogger.com