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Ashburn, Bradley O., Carter, Rich G., Zakharov, Lev N. (2007) Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels−Alder Approach. Journal Of The American Chemical Society, 129 (29) 9109-9116 doi:10.1021/ja071163r

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels−Alder Approach
JournalJournal Of The American Chemical Society
AuthorsAshburn, Bradley O.Author
Carter, Rich G.Author
Zakharov, Lev N.Author
Year2007 (July)Volume129
Issue29
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja071163rSearch in ResearchGate
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Mindat Ref. ID1685428Long-form Identifiermindat:1:5:1685428:4
GUID0
Full ReferenceAshburn, Bradley O., Carter, Rich G., Zakharov, Lev N. (2007) Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels−Alder Approach. Journal Of The American Chemical Society, 129 (29) 9109-9116 doi:10.1021/ja071163r
Plain TextAshburn, Bradley O., Carter, Rich G., Zakharov, Lev N. (2007) Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels−Alder Approach. Journal Of The American Chemical Society, 129 (29) 9109-9116 doi:10.1021/ja071163r
In(2007, July) Journal Of The American Chemical Society Vol. 129 (29) American Chemical Society (ACS)

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Ashburn, Bradley O., Carter, Rich G. (2006) Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri- and Tetra-ortho-substituted Phosphorus-Containing Biaryls. Angewandte Chemie, 118 (40). 6889-6893 doi:10.1002/ange.200602683
Ashburn, Bradley O., Carter, Rich G. (2006) Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri- and Tetra-ortho-substituted Phosphorus-Containing Biaryls. Angewandte Chemie International Edition, 45 (40). 6737-6741 doi:10.1002/anie.200602683
Perkins, Johanna R., Carter, Rich G. (2008) Synthesis of Programmable Tetra-ortho-Substituted Biaryl Compounds Using Diels−Alder Cycloadditions/Cycloreversions of Disubstituted Alkynyl Stannanes. Journal Of The American Chemical Society, 130 (11) 3290-3291 doi:10.1021/ja7113486
Yang, Hua, Carter, Rich G., Zakharov, Lev N. (2008) Enantioselective Total Synthesis of Lycopodine. Journal Of The American Chemical Society, 130 (29) 9238-9239 doi:10.1021/ja803613w
Zhang, , Bruice, Thomas C. (2007) Diels−Alder Ribozyme Catalysis:  A Computational Approach. Journal Of The American Chemical Society, 129 (4) 1001-1007 doi:10.1021/ja067416i
Yang, He, Sun, Jiawei, Gu, Wei, Tang, Wenjun (2020) Enantioselective Cross-Coupling for Axially Chiral Tetra-ortho-Substituted Biaryls and Asymmetric Synthesis of Gossypol. Journal of the American Chemical Society, 142 (17) 8036-8043 doi:10.1021/jacs.0c02686
Payette, Joshua N., Yamamoto, Hisashi (2007) Regioselective and Asymmetric Diels−Alder Reaction of 1- and 2-Substituted Cyclopentadienes Catalyzed by a Brønsted Acid Activated Chiral Oxazaborolidine. Journal Of The American Chemical Society, 129 (31) 9536-9537 doi:10.1021/ja0735958
McBee, E. T., Hsu, C. G., Pierce, O. R., Roberts, C. W. (1955) Diels-Alder Reactions with Fluorine-containing Olefins. Journal Of The American Chemical Society, 77 (4) 915-917 doi:10.1021/ja01609a034
Yuan, Changchun, Du, Biao, Yang, Li, Liu, Bo (2013) Bioinspired Total Synthesis of Bolivianine: A Diels– Alder/Intramolecular Hetero-Diels–Alder Cascade Approach. Journal Of The American Chemical Society, 135 (25) 9291-9294 doi:10.1021/ja4040335
Dai, Mingji, Sarlah, David, Yu, Maolin, Danishefsky, Samuel J., Jones, Gavin O., Houk, K. N. (2007) Highly Selective Diels-Alder Reactions of Directly Connected Enyne Dienophiles. Journal Of The American Chemical Society, 129 (3) 645-657 doi:10.1021/ja065762u
Lenhert, P. Galen., Lukehart, C. M., Sacksteder, LouAnn. (1986) Reactions of coordinated molecules. 42. Diels-Alder reactions utilizing (ferra-.beta.-diketonato)difluoroboron complexes containing alkenyl substituents as activated dienophiles. Journal Of The American Chemical Society, 108 (4) 793-800 doi:10.1021/ja00264a036
 
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