Lista de obras - Paul Lloyd-Williams - Dominio Público Uruguay

A Useful Allene for the Stereoselective Synthesis of Protected Quaternary 2-Amino-2-vinyl-1,3-diols.

artículo científico publicado en 2017

Analysis of conformational equilibria in aplidine using selective excitation 2D NMR spectroscopy and molecular mechanics/dynamics calculations

artículo científico publicado en 2003

Arylboronic acids and arylpinacolboronate esters in Suzuki coupling reactions involving indoles. Partner role swapping and heterocycle protection

artículo científico publicado en 2004

Convergent solid-phase peptide synthesis

article

Convergent solid-phase peptide synthesis. X. Synthesis and purification of protected peptide fragments using the photolabile Nbb-resin

Convergent solid-phase peptide synthesis. XI. Synthesis and purification of protected peptide segments spanning the entire sequence of the uteroglobin monomer using the photolabile nbb-resin

Designed asymmetric coordination helicates with bis-β-diketonate ligands

scientific article published on 04 November 2019

Molecules Designed to Contain Two Weakly Coupled Spins with a Photoswitchable Spacer

artículo científico publicado en 2017

Racemization in suzuki couplings: a quantitative study using 4-hydroxyphenylglycine and tyrosine derivatives as probe molecules

scientific article published on 01 February 2007

Severe side-reaction in the acidolytic cleavage of a C-terminal Met-containing peptide from the solid support. Formation of the homoserine lactone peptide

Simple methods for the preparation of protected derivatives of and

Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides

scholarly article by Paul Lloyd-Williams et al published June 1994 in Tetrahedron Letters

Solid-phase synthesis of peptides using allylic anchoring groups. An investigation of their palladium-catalysed cleavage

scholarly article by Paul Lloyd-Williams et al published August 1991 in Tetrahedron Letters

Synthesis of derivatives of (2S,4S)-4-hydroxy-2,5-dimethyl-3-oxohexanoic acid, a constituent of the didemnins

Synthesis, conformational analysis, and cytotoxicity of conformationally constrained aplidine and tamandarin A analogues incorporating a spirolactam beta-turn mimetic.