๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Encyclopedia of Reagents for Organic Synthesis || 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride

โœ Scribed by Kitamura, Masanori


Book ID
121841837
Publisher
John Wiley & Sons, Ltd
Year
2013
Tongue
English
Weight
247 KB
Category
Article
ISBN-13
9780470842898

No coin nor oath required. For personal study only.

โœฆ Synopsis


Contains A Database Of Approximately 70,000 Reactions And 4000 Of The Most Frequently Consulted Reagents. Fully Searchable By Structure And Sub-structure, Reagent, Reaction Type, Experimental Conditions, And Keyword. Also Includes A Searchable Interface: Acronym Finder (an Interface For Scientific And Technical Acronyms, Symbols, And Abbreviations).


๐Ÿ“œ SIMILAR VOLUMES


Synthesis and characterization of 4-(4,6
โœ Munetaka Kunishima; Chiho Kawachi; Fumiaki Iwasaki; Keiji Terao; Shohei Tani ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 209 KB

4-(4,6-Dimethoxy-l,3,5-triazin-2-yl)-4-methylmotpholinium chloride (DMTMM) was quantitatively synthesized by the coupling of 2-chloro-4,6-dimethoxy-13,5-uiazine and N-methylmorpholine in THF, and fully characterized. Condensation of carboxylic acids and amines by DMTMM proceeded effectivdy in THF to

Encyclopedia of Reagents for Organic Syn
โœ Coffey, D. Scott ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley & Sons, Ltd ๐ŸŒ English โš– 163 KB

Contains A Database Of Approximately 70,000 Reactions And 4000 Of The Most Frequently Consulted Reagents. Fully Searchable By Structure And Sub-structure, Reagent, Reaction Type, Experimental Conditions, And Keyword. Also Includes A Searchable Interface: Acronym Finder (an Interface For Scientific A

Synthesis of sterically-hindered peptido
โœ Wen-Chung Shieh; Zhuoliang Chen; Song Xue; Joe McKenna; Run-Ming Wang; Kapa Pras ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 181 KB

Our study demonstrated that 4-(4,6-dimethoxy-1,3,5-triazine-2-yl)-4-methyl-morpholinium chloride (DMTMM) is a versatile coupling reagent for the synthesis of sterically-hindered peptidomimetics. It is superior to HBTU/HOBt and CDMT in controlling racemization and N-arylation, respectively.