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Total synthesis of (+)-anamarine

โœ Scribed by Kumar, Krishnammagari Suresh; Reddy, Cirandur Suresh


Book ID
120643714
Publisher
Royal Society of Chemistry
Year
2012
Tongue
English
Weight
197 KB
Volume
10
Category
Article
ISSN
1477-0520

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๐Ÿ“œ SIMILAR VOLUMES


A convergent total synthesis of (โˆ’)-anam
โœ Frieder W Lichtenthaler; Klaus Lorenz; Wei-yong Ma ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 290 KB

The di-acetonide of 6-deoxy-aLdehydo-D-qlucose Lz and (S,S)-2-ethoxy-6-triphenylphosphoniomethyl-dihydropyran iodide 2 are elaborated from D-glucose each in practicable procedures of 5 and 10 steps, resp., and subsequently joined to give, after oxidation, deprotection and acetylation, (-I-anamarine

Stereoselective Synthesis of Anamarine.
โœ Santiago Diaz-Oltra; Juan Murga; Eva Falomir; Miguel Carda; J. Alberto Marco ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons โš– 85 KB ๐Ÿ‘ 1 views
A convergent total synthesis of (+)-anam
โœ Klaus Lorenz; Frieder W. Lichtenthaler ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 277 KB

The (R R)-6-alkoxy-2-triphenylphosphoniomethyl-dihydropyran iodide 2 and the --di-acetonide of 6-deoxy-aldehydo-L-glucose 3 are elaborated from (R,R)-tartrate and D-gulonolactone, resp., and subsequently joined to yield (+)-anamarine (l), identical with the Hyptis-derived product.