Search Results - "Cayzer, N."

Polymineralic orientation analysis of magmatic rocks using Electron Back-Scatter Diffraction: Implications for igneous fabric origin and evolution by Romeo, I., Capote, R., Lunar, R., Cayzer, N.

“…Electron Back-Scatter Diffraction (EBSD), which provides an easy way of acquiring large numbers of individual crystallographic orientation data from different…”
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Alkali feldspar microtextures as provenance indicators in siliciclastic rocks and their role in feldspar dissolution during transport and diagenesis by Parsons, Ian, Thompson, Pauline, Lee, Martin R, Cayzer, Nicola

“…Alkali feldspars usually exhibit optical or sub-optical inter-growths of albite and K-feldspar (known generically as perthite) which have morphologies and…”
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Intramolecular Diels−Alder Reactions of Ester-Linked 1,3,8-Nonatrienes by Cayzer, Tory N, Paddon-Row, Michael N, Moran, Damian, Payne, Alan D, Sherburn, Michael S, Turner, Peter

“…Penta-1,3-dienyl acrylates undergo kinetically controlled intramolecular Diels−Alder (IMDA) reactions and DFT calculations (B3LYP/6-31+G(d)) predict…”
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Optimising Stereoselectivity in Intramolecular Diels-Alder Reactions of Pentadienyl Acrylates: Synthetic and Computational Investigations into the "Steric Directing Group" Approach by Cayzer, Tory N., Wong, Leon S.-M., Turner, Peter, Paddon-Row, Michael N., Sherburn, Michael S.

“…Experimental conditions for the intramolecular cycloaddition of four related pentadienyl acrylates 3, 4, 5 and 6 are reported. In contrast with several…”
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Stereocontrol of the Intramolecular Diels−Alder Reaction by Internal Hydrogen Bonding by Cayzer, Tory N., Paddon-Row, Michael N., Sherburn, Michael S.

“…A novel approach for exo/endo stereocontrol of intramolecular Diels−Alder reactions is described. Substrates carrying a hydroxymethyl group attached to the…”
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Stereocontrol of intramolecular Diels-Alder reactions by an allylic diphenylcyclopropyl group by Tripoli, Regis, Cayzer, Tory N, Willis, Anthony C, Sherburn, Michael S, Paddon-Row, Michael N

“…Intramolecular Diels-Alder reactions of ester-linked 1,3,8-nonatrienes carrying a diphenylcyclopropyl substituent attached to C1 proceed with high levels of…”
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