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Angewandte Chemie (International Ed. in English)|January 30, 2015
Anomalous nuclear Overhauser effects in carbon-substituted aziridines: scalar cross-relaxation of the first kindIlya Kuprov, David M Hodgson, Johannes Kloesges, et al.
Organic & Biomolecular Chemistry|June 18, 2009
Synthesis of regio- and stereoselectively deuterium-labelled derivatives of L-glutamate semialdehyde for studies on carbapenem biosynthesisChristian Ducho, Refaat B Hamed, Edward T Batchelar, et al.
Organic & Biomolecular Chemistry|December 17, 2008
Synthesis and conformational analysis of cyclic analogues of inverse gamma-turnsMorakot Kaewpet, Barbara Odell, Michael A King, et al.
The Journal of Organic Chemistry|May 6, 2016
Scalar Cross-Relaxation Detected in the NOESY Spectra of Oxazolidines and ThiazolidinesTharindi D Panduwawala, Laia Josa-Culleré, Ilya Kuprov, et al.
Organic Letters|February 28, 2003
Biomimetic synthesis of the crispatene coreJohn E Moses, Jack E Baldwin, Rodolfo Marquez, et al.
Angewandte Chemie (International Ed. in English)|May 24, 2016
Synthesis of Five-Porphyrin Nanorings by Using Ferrocene and Corannulene TemplatesPengpeng Liu, Yutaka Hisamune, Martin D Peeks, et al.
Journal of the American Chemical Society|February 1, 2014
Synthetic control of retinal photochemistry and photophysics in solutionGiovanni Bassolino, Tina Sovdat, Matz Liebel, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 20, 2012
Synthesis of 3-fluoropyrrolidines and 4-fluoropyrrolidin-2-ones from allylic fluoridesLorraine E Combettes, Marie Schuler, Rakesh Patel, et al.
Chemical Communications (Cambridge, England)|August 9, 2016
Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketiminesRaquel de la Campa, Adam D Gammack Yamagata, Irene Ortín, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 20, 2012
Conformational analysis of fluorinated pyrrolidines using 19F-1H scalar couplings and heteronuclear NOEsLorraine E Combettes, Philip Clausen-Thue, Michael A King, et al.
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