Preferential hydrogenolysis of NAP esters provides a new orthogonal protecting group strategy for carboxylic acids

Tetrahedron Letters

Volumn 40, Issue 9, 1999, Pages 1803-1806

  Gaunt, Matthew J ^a   Boschetti, Carlos E ^a   Yu, Jinquan ^a   Spencer, Jonathan B ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

2 NAPHTHYLMETHYL ESTER; 4 TRIFLUOROMETHYLBENZYL DERIVATIVE; DICARBOXYLIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; HYDROGEN BOND; ORGANIC CHEMISTRY; PEPTIDE ANALYSIS; REACTION ANALYSIS; STRUCTURE ANALYSIS;

EID: 0033605180     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00014-3     Document Type: Article

References (10)

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9. [9] All new compounds were characterised by 250 or 500 MHz NMR and high resolution mass spectrometry.
10. [10] Hassner A, Alexanian V. Tetrahedron Lett. 1978;4475-4478.