Stereochemistry of lactide polymerization with chiral catalysts: new opportunities for stereocontrol using polymer exchange mechanisms.

By Tina M. Ovitt, G. Coates. Journal of the American Chemical Society, 2002

635 citations recorded by the source corpus.

Subfields: Biomaterials, Organic Chemistry, Process Chemistry and Technology

View Paper: https://www.semanticscholar.org/paper/ceda49cdf020a82ac89a3159eb87fedb4d9adad0

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In Biomaterials

1. Charlotte K. Williams
2. L. M. Hodgson
3. Rachel H. Platel

In Organic Chemistry

1. Charlotte K. Williams
2. L. M. Hodgson
3. Rachel H. Platel

In Process Chemistry and Technology

1. Charlotte K. Williams
2. L. M. Hodgson
3. Rachel H. Platel

Citations in the corpus

• Biocompatible Initiators for Lactide Polymerization (2008, methodology): “copoly((R-LA)n-b-(SLA)n) on the basis of the stereoerrors observed in the proton decoupled (1)H NMR and a re-evaluation of the calorimetry.(97,139) A polymer exchange mechanism was proposed to explain the stereoblock formation (Fig.”