Quezada V, Castroagudin M, Verdugo F, Ortiz S, Zaragoza G, Nachtigall F
Molecules. 2024; 29(7).
PMID: 38611883
PMC: 11013886.
DOI: 10.3390/molecules29071604.
Xu J
Molecules. 2024; 29(7).
PMID: 38611737
PMC: 11012711.
DOI: 10.3390/molecules29071454.
Zhang R, Xia Y, Dong G
Angew Chem Int Ed Engl. 2021; 60(37):20476-20482.
PMID: 34216095
PMC: 8405584.
DOI: 10.1002/anie.202106007.
Connon R, Roche B, Rokade B, Guiry P
Chem Rev. 2021; 121(11):6373-6521.
PMID: 34019404
PMC: 8277118.
DOI: 10.1021/acs.chemrev.0c00844.
Andreev I, Ratmanova N, Augustin A, Ivanova O, Levina I, Khrustalev V
Angew Chem Int Ed Engl. 2021; 60(14):7927-7934.
PMID: 33433034
PMC: 8048580.
DOI: 10.1002/anie.202016593.
Recent Developments in Enantioselective Transition Metal Catalysis Featuring Attractive Noncovalent Interactions between Ligand and Substrate.
Fanourakis A, Docherty P, Chuentragool P, Phipps R
ACS Catal. 2020; 10(18):10672-10714.
PMID: 32983588
PMC: 7507755.
DOI: 10.1021/acscatal.0c02957.
Uncovering the Neglected Similarities of Arynes and Donor-Acceptor Cyclopropanes.
Werz D, Biju A
Angew Chem Int Ed Engl. 2019; 59(9):3385-3398.
PMID: 31529661
PMC: 7065169.
DOI: 10.1002/anie.201909213.
Catalytic asymmetric cycloaddition reactions of enoldiazo compounds.
Marichev K, Doyle M
Org Biomol Chem. 2019; 17(17):4183-4195.
PMID: 30924829
PMC: 6484446.
DOI: 10.1039/c9ob00478e.
Cycloaddition reactions of enoldiazo compounds.
Cheng Q, Deng Y, Lankelma M, Doyle M
Chem Soc Rev. 2017; 46(17):5425-5443.
PMID: 28726896
PMC: 5575991.
DOI: 10.1039/c7cs00324b.
Switchable selectivity in an NHC-catalysed dearomatizing annulation reaction.
Guo C, Fleige M, Janssen-Muller D, Daniliuc C, Glorius F
Nat Chem. 2015; 7(10):842-7.
PMID: 26391085
DOI: 10.1038/nchem.2337.
One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.
Liu Q, Yan W, Wang L, Zhang X, Tang Y
Org Lett. 2015; 17(16):4014-7.
PMID: 26252859
PMC: 4746102.
DOI: 10.1021/acs.orglett.5b01909.
The [3 + 3]-cycloaddition alternative for heterocycle syntheses: catalytically generated metalloenolcarbenes as dipolar adducts.
Xu X, Doyle M
Acc Chem Res. 2014; 47(4):1396-405.
PMID: 24650430
PMC: 3993878.
DOI: 10.1021/ar5000055.
Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates.
Xu X, Zavalij P, Doyle M
Angew Chem Int Ed Engl. 2013; 52(48):12664-8.
PMID: 24123489
PMC: 3858852.
DOI: 10.1002/anie.201305539.