The facile conversion of T-2 toxin and neosolaniol into anguidine
โ Scribed by Derek W Anderson; Robin M Black; David A Leigh; J.Fraser Stoddart; Nancy E. Williams
- Book ID
- 104227638
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 207 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
S3 7HF
T-2 Toxin (5) and neosolaniol ( 6) are readily converted into anguidine 11) by a procedure where deoxygenation at the C-8 position is achieved, after conversion of the 3-TBDMS ether 7 of neosolaniol ( 6) to the 8-bromide 11 for reduction to the anguidine precursor 12.
Amongst the trichothecene group of antibiotics, anguidine (1) is a key compound as a result of its ready conversion lr2 into verrucarol (2) -the
๐ SIMILAR VOLUMES
A facile one-pot synthesis of amides from aldehydes has been developed. This tandem process involves the formation of a nitrile intermediate obtained from the reaction of an aldehyde with hydroxylamine hydrochloride in dimethylsulfoxide at 100 C and the subsequent treatment of the nitrile with basic