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144Marco Lucarini and Gian Franco Pedulli.
Free radical intermediates in the inhibition of the autoxidation reaction, Chem. Soc. Rev., 2010, 39, 2106. Tao Zeng and Ju-Feng Sun .
2,6-Di-tert-butyl-4-(methoxymethyl)phenol , Acta Cryst (2008). E64, o588Â Â M. Lutz and A. L. Spek.
2,6-Di-tert-butylphenol revisited at 110 K, Acta Cryst. (2005). C61, o639-o641Â Â Â Â Jean-Damien Charrier, James E. S. Duffy, Peter B. Hitchcock and Douglas W. Young.
Unusual stereoselectivity in the alkylation of pyroglutamate ester urethanes, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 2367. Garth R. Giesbrecht, Glenn D. Whitener and John Arnold.
Mono-guanidinate complexes of lanthanum: synthesis, structure and their use in lactide polymerization, Dalton Trans., 2001, 0, 923. Anil Wali, Jagannath Das, S. Muthukumaru Pillai and M. Ravindranathan.
Disproportionation, isomerization and de-tert-butylation of 2,6-di-tert-butylphenol catalyzed by H-MCM-41, Green Chem., 2002, 4, 587. Stephen G. Davies, A. Christopher Garner, Marcus J. C. Long, Andrew D. Smith, Miles J. Sweet and Jonathan M. Withey.
Parallel kinetic resolution of tert-butyl (RS)-3-alkyl–cyclopentene-1-carboxylates for the asymmetric synthesis of 3-alkyl–cispentacin derivatives, Org. Biomol. Chem., 2004, 2, 3355. Sarika Sharma, Boris Kerler, Bala Subramaniam and A. S. Borovik.
Immobilized metal complexes in porous hosts: catalytic oxidation of substituted phenols in CO media, Green Chem., 2006, 8, 972. Ming Wei, Ghezai T. Musie, Daryle H. Busch and Bala Subramaniam.
Autoxidation of 2,6-di-tert-butylphenol with cobalt Schiff base catalysts by oxygen in CO-expanded liquids, Green Chem., 2004, 6, 387. Julio G. Urones, Narciso M. Garrido, David Díez, Mohamed M. El Hammoumi, Sara H. Dominguez, J. Antonio Casaseca, Stephen G. Davies and Andrew D. Smith.
Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate, Org. Biomol. Chem., 2004, 2, 364.