2-Naphthalenesulfonyl as a Tosyl Substitute for Protection of Amino Functions. Cyclic Voltammetry Studies on Model Sulfonamides and Their Preparative Cleavage by Reduction
- 31 August 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (19), 7135-7139
- https://doi.org/10.1021/jo990695q
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Deprotection of Sulfonyl AziridinesThe Journal of Organic Chemistry, 1998
- Neighbouring group assisted sulfonamide cleavage of Sharpless aminols under acetonation conditionsTetrahedron Letters, 1998
- A Practical Reagent for the Synthesis of Substituted HydrazinesSynthesis, 1997
- Desulfonylation of Amides Using Samarium IodideSynlett, 1997
- Mild, efficient cleavage of arenesulfonamides by magnesium reductionChemical Communications, 1997
- Stepwise synthesis of tetrasubstituted hydrazinesChemical Communications, 1997
- Protection of Amines by the Pyridine-2-sulfonyl Group and Its Cleavage under Mild Conditions (SmI2 or Electrolysis)The Journal of Organic Chemistry, 1995
- Optically Active Total Synthesis of Clavicipitic AcidThe Journal of Organic Chemistry, 1995
- Deprotection of Arenesulfonamides with Samarium iodideThe Journal of Organic Chemistry, 1994
- Selective cathodic cleavage of unsymmetrical imidodicarbonates, acylcarbamates and diacylamidesJournal of the Chemical Society, Perkin Transactions 2, 1993