Spicing up olefin cross metathesis with the renewables estragole and methyl sorbate
Tài liệu tham khảo
Grela, 2014
dos Santos, 2018, 230
Ho, 2009, ChemSusChem, 2, 749, 10.1002/cssc.200900091
Rybak, 2007, Green Chem., 12, 1356, 10.1039/b712293d
Ferreira, 2016, Catal. Sci. Technol., 6, 8138, 10.1039/C6CY01181K
Duque, 2011, Green Chem., 13, 1187, 10.1039/c1gc15048k
Behr, 2014, RSC Adv., 4, 16320, 10.1039/C3RA47671E
Behr, 2011, Eur. J. Lipid Sci. Technol., 113, 189, 10.1002/ejlt.201000299
Granato, 2017, ChemSusChem, 10, 1832, 10.1002/cssc.201700116
Lummiss, 2012, J. Am. Chem. Soc., 134, 18889, 10.1021/ja310054d
Prunet, 2010
Bilel, 2020, ChemCatChem, 12, 5000, 10.1002/cctc.202000959
Ferrié, 2007, Synlett., 18, 2891
Ferrié, 2006, J. Organomet. Chem., 691, 5456, 10.1016/j.jorganchem.2006.09.026
Funk, 2005, Org. Lett., 7, 187, 10.1021/ol047929z
Krishna, 2008, Tetrahedron Lett., 49, 2013, 10.1016/j.tetlet.2008.01.055
Saraçi, 2018, ChemSusChem, 11, 773, 10.1002/cssc.201701874
Moura-Letts, 2007, Org. Lett., 9, 5, 10.1021/ol062017d
Dewi, 2005, Tetrahedron Lett., 46, 577, 10.1016/j.tetlet.2004.11.154
Jeon, 2019, Appl. Biol. Chem., 62, 1
Venkateshwarlu, 2017, Med. Chem. Commun., 8, 394, 10.1039/C6MD00606J
Oláh, 2017, Phytomedicine, 34, 44, 10.1016/j.phymed.2017.06.006
Cookson, 2014, Eur. J. Org. Chem., 21, 4523, 10.1002/ejoc.201402205
Albrecht, 2019, Org. Biomol. Chem., 17, 4238, 10.1039/C9OB00386J
Riveira, 2018, Org. Lett., 20, 4000, 10.1021/acs.orglett.8b01567
Dada, 2018, Angew. Chem. Int. Ed., 57, 3981, 10.1002/anie.201800361
Marsili, 2018, Org. Lett., 20, 7298, 10.1021/acs.orglett.8b03229
Gao, 2018, Chem. Commun., 54, 3601, 10.1039/C8CC01201F
Uraguchi, 2017, Nat. Commun., 8, 14793, 10.1038/ncomms14793
Wu, 2016, Adv. Synth. Catal., 358, 2510, 10.1002/adsc.201600375
Wang, 2015, Chem. Eur. J., 21, 7709, 10.1002/chem.201500833
Sawano, 2012, J. Am. Chem. Soc., 134, 18936, 10.1021/ja309756k
Okada, 2008, Angew. Chem. Int. Ed., 47, 6860, 10.1002/anie.200801928
Fukuhara, 2005, Tetrahedron Lett., 46, 603, 10.1016/j.tetlet.2004.11.131
Herrán, 2005, Org. Lett., 7, 5629, 10.1021/ol0522485
Davis, 1999, J. Chem. Soc. Perkin Trans. I, 3089, 10.1039/a907017f
Quijia, 2020, Crit. Rev. Anal. Chem., 50, 62, 10.1080/10408347.2019.1573656
Salehi, 2019, Molecules, 24, 1364, 10.3390/molecules24071364
Further conversion of the methyl ester to other functional groups, such as amides, can be accomplished using well-stablished literature protocols. For a green chemistry perspective on catalytic amide bond formation, see: M.T. Sabatini, L.T. Boulton, H.F. Sneddon, T.D. Sheppard, Nature Catal. 2 (2019) 10-17. https://doi.org/10.1038/s41929-018-0211-5.
Bailey, 2015, J. Am. Chem. Soc., 137, 7318, 10.1021/jacs.5b04524
Santos, 2017, ACS Catal., 7, 3181, 10.1021/acscatal.6b03557
Bieniek, 2008, Chem. Eur. J., 14, 806, 10.1002/chem.200701340
Bourgeois, 2002, J. Organomet. Chem., 643-644, 247, 10.1016/S0022-328X(01)01269-4
Ashworth, 2012, Eur. J. Org. Chem., 29, 5673, 10.1002/ejoc.201201036