Results 1 - 10 of 474

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Ikuro Abe and Hiroyuki Morita. Structure and function of the chalcone synthase superfamily of plant type III polyketide synthases, Nat. Prod. Rep., 2010, 27, 809.
[DOI: 10.1039/b909988n]
A. Degen and M. Bolte. 4-Phenylbut-3-en-2-one (benzalacetone), Acta Cryst. (1999). C55, IUC9900170Â Â Â Â
[DOI: 10.1107/S0108270199098236]
L. Wang, L. Peng, J. Bai, Q. Huang, X. Xu and L. Wang. Highly organocatalytic asymmetric Michael–ketone aldol–dehydration domino reaction: straightforward approach to construct six-membered spirocyclic oxindoles, Chem. Commun., 2010
[DOI: 10.1039/c0cc03032e]
Xuefeng Li, Lingfeng Cun, Chunxia Lian, Ling Zhong, Yingchun Chen, Jian Liao, Jin Zhu and Jingen Deng. Highly enantioselective Michael addition of malononitrile to α,β-unsaturated ketones, Org. Biomol. Chem., 2008, 6, 349.
[DOI: 10.1039/b713129a]
Tai-Ran Kang, Jian-Wu Xie, Wei Du, Xin Feng and Ying-Chun Chen. Stereoselective desymmetrisation of prochiral α,α-dicyanoalkenes via domino Michael–Michael addition reactions, Org. Biomol. Chem., 2008, 6, 2673.
[DOI: 10.1039/b809308c]
Anirban Sarkar, Sudipta Raha Roy and Asit K. Chakraborti. Ionic liquid catalysed reaction of thiols with α,β-unsaturated carbonyl compounds—remarkable influence of the C-2 hydrogen and the anion, Chem. Commun., 2011, 47, 4538.
[DOI: 10.1039/c1cc10151j]
Daniela Lanari, Roberto Ballini, Simona Bonollo, Alessandro Palmieri, Ferdinando Pizzo and Luigi Vaccaro. JandaJel as a polymeric support to improve the catalytic efficiency of immobilized-1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) under solvent-free conditions, Green Chem., 2011, 13, 3181.
[DOI: 10.1039/c1gc15790f]
Bin Cao, Yong Wang, Kan Ding, Nouri Neamati and Ya-Qiu Long. Synthesis of the pyridinyl analogues of dibenzylideneacetone (pyr-dba) via an improved Claisen–Schmidt condensation, displaying diverse biological activities as curcumin analogues, Org. Biomol. Chem., 2012, 10, 1239.
[DOI: 10.1039/c1ob06773g]
Craig M. Comisar and Phillip E. Savage. Kinetics of crossed aldol condensations in high-temperature water, Green Chem., 2004, 6, 227.
[DOI: 10.1039/b314622g]
John H. MacMillan Stephen S. Washburne. Lanthanide Chemical Shift Reagents as Tools for Determining Isomer Distributions in 2,4-Hexadieneoates and Related Compounds, Organic Magnetic Resonance, Vol. 6, p250, (1974).
[DOI: 10.1002/mrc.1270060414]
The isomer distributions in Me sorbate, 2,4-hexadienol, PhCH:CHCOMe and Me cinnamate were detd. from their NMR spectra with Eu(fod)3 (fod= 1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato). The method was est. to detect the presence of ~2% of a cis isomer