Andrew F. Kyle

Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis

R. Schrock, D. Dixon, Miao Yu, 2011, Nature.

In Vitro and In Vivo Evaluation of Cysteine Rebridged Trastuzumab-MMAE Antibody Drug Conjugates with Defined Drug-to-Antibody Ratios.

J. Choi, M. Bird, W. McDowell, 2015, Molecular pharmaceutics.

Efficient and selective formation of macrocyclic disubstituted Z alkenes by ring-closing metathesis (RCM) reactions catalyzed by Mo- or W-based monoaryloxide pyrrolide (MAP) complexes: applications to total syntheses of epilachnene, yuzu lactone, ambrettolide, epothilone C, and nakadomarin A.

R. Schrock, D. Dixon, Miao Yu, 2013, Chemistry.

Catalytic asymmetric alkylation reactions for the construction of protected ethylene-amino and propylene-amino motifs attached to quaternary stereocentres.

T. Moss, D. Dixon, D. M. Barber, 2013, Chemistry.

Bridging disulfides for stable and defined antibody drug conjugates.

M. Bird, M. Fisher, A. Godwin, 2014, Bioconjugate chemistry.

Applications of NHC-mediated O- to C-carboxyl transfer: synthesis of (±)-N-benzyl-coerulescine and (±)-horsfiline

A. Slawin, Andrew D. Smith, Kenneth B. Ling, 2010 .

Modulation of drug‐linker design to enhance in vivo potency of homogeneous antibody‐drug conjugates

P. Williams, M. Bird, A. Jenkins, 2017, Journal of controlled release : official journal of the Controlled Release Society.