Study of metal and acid catalysed deprotection of propargyl ethers of alcohols via their allenyl ethers
โ Scribed by Hari Babu Mereyala; Srinivas Reddy Gurrala; S Krishna Mohan
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 795 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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โฆ Synopsis
A new method for the deprotection of prop-2-ynyl ethers lb-9b is described.
Isomerisation of lb-9b to O-allenyl ethers ld-9d and deprotection by reaction with Hg(OCOCF3)2, aq.HCl, aq.CF3CO2H and best by use of a catalytic amount of OsO4 is described to obtain the alcohols la-9a in good yield. Application of this method for the deprotection of prop-2-enyl ethers 7c,8c,10ยข-13ยข via their corresponding prop-l-enyl ethers 7e,8e,10e-13e to obtain the corresponding alcohols 7a,8a,10a-13a is also described.
๐ SIMILAR VOLUMES
## Abstract A new type of crown ethers containing a diphenyl ether unit has been prepared, the ring size ranging from 12 to 36. ^1^H and ^13^C NMR spectra of both free ligands and their metalโion complexes have been recorded. For 18โ and 21โmembered compounds a general downfield shift was observed
Two thiacrown ethers with pendant carboxylic acid groups, 3,6,10,13-tetrathiacyclotetradec-1-oxyacetic acid (TTCTOAA) and 2-(3,6,10,13-tetrathiacyclotetradec-l-oxy)hexanoic acid (TKTOHA), were synthesized and their proton dissociation constants (p&Y,) were determined potentiometrically at 25 + O.l"C