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Recent developments in chemical deprotection of ester functional groups

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Recent developments in chemical deprotection of ester functional groups (English)

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author name string

Claudio J. Salomon

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1

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Ernesto G. Mata

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Oreste A. Mascaretti

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3

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publication date

April 1993

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published in

Tetrahedron

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volume

49

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issue

18

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page(s)

3691-3734

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Hard and Soft Acids and Bases

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Ortho bromination of phenols

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Absolute hardness: companion parameter to absolute electronegativity

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Application of Pig Liver Esterases (PLE) in Asymetric Synthesis

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Peptide alkaloids of Discaria longispina

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Iodotrimethylsilane—a versatile synthetic reagent

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Bis (tributyltin) oxide. A mild, neutral and selective reagent for cleavage of esters. Scope and limitation of the reaction

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Allyl esters as carboxy protecting groups in the synthesis of O-glycopeptides

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Asymmetric oxidation of ester and amide enolates using new (camphorylsulfonyl)oxaziridines

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GR 20263, a new broad-spectrum cephalosporin with anti-pseudomonal activity

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DOI

10.1016/S0040-4020(01)90225-X

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(Q58854085)

Recent developments in chemical deprotection of ester functional groups

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