L-Selectride as a convenient reagent for the selective cleavage of carbamates
β Scribed by Andrew Coop; Kenner C. Rice
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 135 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Diallyldicarbonate was prepared and used for the amino protection of various compounds including amino acids, amino sugars and nucleosides.
L-Selectride as a General Reagent for the O-Demethylation and N-Decarbomethoxylation of Opium Alkaloids and Derivatives. -L-Selectride is shown to be an efficient O-demethylating reagent for the opium alkaloids and an efficient reagent for the cleavage of methyl carbamates, thus offering a convenie
Ababuctz nle selective clesvage ofprimary sml secondsty trimethylsilyl (TMS). abopmpylsilyl (TIPS), tut-butyldimahylsilyl~DMS)rrndtut-butyldiphnylsilyl~DPS)ahaswithwrtral~urminr\mdaverymildconditions is described. The method involvea tdiktkm of the support, pwiously activated by hesting at WC/O. 1 t