Aloiau A, Bobek B, Caddell Haatveit K, Pearson K, Watkins A, Jones B
J Org Chem. 2024; 89(6):3875-3882.
PMID: 38422508
PMC: 10949245.
DOI: 10.1021/acs.joc.3c02723.
Nagamalla S, Thomas A, Nirpal A, Mague J, Sathyamoorthi S
J Org Chem. 2023; 88(22):15989-16006.
PMID: 37903411
PMC: 10799289.
DOI: 10.1021/acs.joc.3c01731.
Malcolmson S, Li K, Shao X
Synlett. 2021; 30(11):1253-1268.
PMID: 33731976
PMC: 7963344.
DOI: 10.1055/s-0037-1611770.
Agrawal T, Martin R, Collins S, Wilhelm Z, Edwards M, Gutierrez O
J Org Chem. 2021; 86(7):5026-5046.
PMID: 33724828
PMC: 8025098.
DOI: 10.1021/acs.joc.0c02971.
Tambe S, Min K, Iqbal N, Cho E
Beilstein J Org Chem. 2020; 16:1335-1342.
PMID: 32595781
PMC: 7308614.
DOI: 10.3762/bjoc.16.114.
2-Unsubstituted Imidazole -Oxides as Novel Precursors of Chiral 3-Alkoxyimidazol-2-ylidenes Derived from -1,2-Diaminocyclohexane and Other Chiral Amino Compounds.
Mloston G, Celeda M, Jasinski M, Urbaniak K, Boratynski P, R Schreiner P
Molecules. 2019; 24(23).
PMID: 31810181
PMC: 6930529.
DOI: 10.3390/molecules24234398.
Enantioselective Organocatalytic Amine-Isocyanate Capture-Cyclization: Regioselective Alkene Iodoamination for the Synthesis of Chiral Cyclic Ureas.
Struble T, Lankswert H, Pink M, Johnston J
ACS Catal. 2019; 8(12):11926-11931.
PMID: 31131150
PMC: 6528665.
DOI: 10.1021/acscatal.8b03708.
Design principles of chiral carbon nanodots help convey chirality from molecular to nanoscale level.
ordevic L, Arcudi F, DUrso A, Cacioppo M, Micali N, Burgi T
Nat Commun. 2018; 9(1):3442.
PMID: 30143608
PMC: 6109168.
DOI: 10.1038/s41467-018-05561-2.
Asymmetric Conjugate Addition of α,α-Disubstituted Aldehydes to Nitroalkenes Organocatalyzed by Chiral Monosalicylamides from trans-Cyclohexane-1,2-Diamines.
Martinez-Guillen J, Flores-Ferrandiz J, Gomez C, Gomez-Bengoa E, Chinchilla R
Molecules. 2018; 23(1).
PMID: 29324713
PMC: 6017890.
DOI: 10.3390/molecules23010141.
Cinchonidinium acetate as a convenient catalyst for the asymmetric synthesis of -stilbenediamines.
Walvoord R, Kozlowski M
Tetrahedron Lett. 2015; 56(23):3070-3074.
PMID: 26041941
PMC: 4450089.
DOI: 10.1016/j.tetlet.2014.12.105.
Application of cyclic phosphonamide reagents in the total synthesis of natural products and biologically active molecules.
Focken T, Hanessian S
Beilstein J Org Chem. 2014; 10:1848-77.
PMID: 25246946
PMC: 4168934.
DOI: 10.3762/bjoc.10.195.
Vicinal diamination of alkenes under Rh-catalysis.
Olson D, Su J, Roberts D, Du Bois J
J Am Chem Soc. 2014; 136(39):13506-9.
PMID: 25233140
PMC: 4183635.
DOI: 10.1021/ja506532h.
Carbanion-accelerated Claisen rearrangements: asymmetric induction with chiral phosphorus-stabilized anions.
Denmark S, Marlin J, Rajendra G
J Org Chem. 2012; 78(1):66-82.
PMID: 23101563
PMC: 3537898.
DOI: 10.1021/jo301919e.
Methods for direct alkene diamination, new & old.
de Jong S, Nosal D, Wardrop D
Tetrahedron. 2012; 68(22):4067-4105.
PMID: 22888177
PMC: 3413304.
DOI: 10.1016/j.tet.2012.03.036.
(S)-N-[(1S,2S)-2-Benzyl-amino-1-(4-hy-droxy-phen-yl)-3-methyl-butyl]-1,1-di-methyl-ethane-2-sulfinamide.
Shen C
Acta Crystallogr Sect E Struct Rep Online. 2011; 64(Pt 11):o2082.
PMID: 21580947
PMC: 2959556.
DOI: 10.1107/S1600536808031073.
[(1R*,2S*)-N-Benzyl-2-phenyl-1-(pyridin-2-yl)-N-(pyridin-2-ylmeth-yl)ethane-1,2-diamine]-dichloridozinc(II).
J Bortoluzzi A, Mireski S, Joussef A
Acta Crystallogr Sect E Struct Rep Online. 2011; 67(Pt 3):m337-8.
PMID: 21522267
PMC: 3052059.
DOI: 10.1107/S1600536811004314.
Catalytic enantioselective aryl transfer to aldehydes using chiral 2,2'-bispyrrolidine-based salan ligands.
Jia X, Lin A, Mao Z, Zhu C, Cheng Y
Molecules. 2011; 16(4):2971-81.
PMID: 21471936
PMC: 6260645.
DOI: 10.3390/molecules16042971.
Synthesis and coordination chemistry of tri-substituted benzamidrazones.
Crimmin M, Colby D, Ellman J, Bergman R
Dalton Trans. 2010; 40(2):514-22.
PMID: 21109860
PMC: 3063360.
DOI: 10.1039/c0dt01267j.
Rapid enantiomeric excess and concentration determination using simple racemic metal complexes.
Nieto S, Lynch V, Anslyn E, Kim H, Chin J
Org Lett. 2008; 10(22):5167-70.
PMID: 18939802
PMC: 2749327.
DOI: 10.1021/ol802085j.