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16,464 results

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Page 1
Showing results for chiral n
Search for Chilal N instead (1 results)
Planar-Chiral Ferrocene-Based N-Heterocyclic Carbene Ligands.
Yoshida K, Yasue R. Yoshida K, et al. Chemistry. 2018 Dec 12;24(70):18575-18586. doi: 10.1002/chem.201803903. Epub 2018 Nov 28. Chemistry. 2018. PMID: 30277615 Review.
This review documents advances in chiral NHC ligands, focusing on planar-chiral ferrocene-based NHCs. As the basic shape of most classes of NHC rings is planar, it seems rational to employ a planar-chiral element in the design of chiral NHC ligands....
This review documents advances in chiral NHC ligands, focusing on planar-chiral ferrocene-based NHCs. As the basic shape of mo …
Axially chiral N-alkyl-N-cinnamoyl amide type P,olefin ligands for Pd-catalyzed reactions.
Mino T, Takaya K, Koki K, Akimoto N, Yoshida Y, Kasashima Y, Sakamoto M. Mino T, et al. Org Biomol Chem. 2023 Mar 29;21(13):2775-2778. doi: 10.1039/d3ob00224a. Org Biomol Chem. 2023. PMID: 36920143
We synthesized N-alkyl-N-cinnamoyl amide type phosphine-olefin compounds 1 and found axial chirality in a C(aryl)-N(amide) bond in compounds 1 by HPLC analysis using a chiral stationary phase column. We successfully obtained enantiomeric isomers …
We synthesized N-alkyl-N-cinnamoyl amide type phosphine-olefin compounds 1 and found axial chirality in a C(aryl)-N
Helical Chiral N-Heterocyclic Carbene Ligands in Enantioselective Gold Catalysis.
Pallova L, Abella L, Jean M, Vanthuyne N, Barthes C, Vendier L, Autschbach J, Crassous J, Bastin S, César V. Pallova L, et al. Chemistry. 2022 Mar 22;28(17):e202200166. doi: 10.1002/chem.202200166. Epub 2022 Feb 28. Chemistry. 2022. PMID: 35143078 Free article.
The first chiral helicene-NHC gold(I) complexes efficient in enantioselective catalysis were prepared. ...The chiral information was introduced in a key post-functionalization step of a NHC-gold(I) complex bearing a symmetrical anionic fluoreno[5]helicene substituen …
The first chiral helicene-NHC gold(I) complexes efficient in enantioselective catalysis were prepared. ...The chiral informati …
Axially chiral N,N'-dioxides ethers for catalysis in enantioselective allylation of aldehydes.
Wu S, Xing Y, Wang J, Guo X, Zhu H, Li W. Wu S, et al. Chirality. 2019 Nov;31(11):947-957. doi: 10.1002/chir.23122. Epub 2019 Aug 28. Chirality. 2019. PMID: 31456306
A series of axially chiral ethers synthesized from biscarboline N,N'-dioxides, (S)-1a to (S)-1n, was investigated in enantioselectivity addition reactions of allyltrichlorosilane with a series of substituted aldehydes, including bulky substituted aldehydes. . …
A series of axially chiral ethers synthesized from biscarboline N,N'-dioxides, (S)-1a to (S)-1n, was investigated in en …
Organocatalytic Atroposelective Synthesis of N-N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation.
Chen KW, Chen ZH, Yang S, Wu SF, Zhang YC, Shi F. Chen KW, et al. Angew Chem Int Ed Engl. 2022 Apr 19;61(17):e202116829. doi: 10.1002/anie.202116829. Epub 2022 Feb 23. Angew Chem Int Ed Engl. 2022. PMID: 35080808
The first highly atroposelective construction of N-N axially chiral indole scaffolds was established via a new strategy of de novo ring formation. ...In addition, this strategy is applicable for the atroposelective synthesis of N-N axially ch
The first highly atroposelective construction of N-N axially chiral indole scaffolds was established via a new strategy …
Catalytic Enantioselective Synthesis of N-C Axially Chiral N-(2,6-Disubstituted-phenyl)sulfonamides through Chiral Pd-Catalyzed N-Allylation.
Fukasawa S, Toyoda T, Kasahara R, Nakamura C, Kikuchi Y, Hori A, Richards GJ, Kitagawa O. Fukasawa S, et al. Molecules. 2022 Nov 13;27(22):7819. doi: 10.3390/molecules27227819. Molecules. 2022. PMID: 36431920 Free PMC article.
Recently, catalytic enantioselective syntheses of N-C axially chiral compounds have been reported by many groups. Most N-C axially chiral compounds prepared through a catalytic asymmetric reaction possess carboxamide or nitrogen-containing aromatic het …
Recently, catalytic enantioselective syntheses of N-C axially chiral compounds have been reported by many groups. Most N
Self-Assembly of Chiral Cyclohexanohemicucurbit[n]urils with Bis(Zn Porphyrin): Size, Shape, and Time-Dependent Binding.
Šakarašvili M, Ustrnul L, Suut E, Nallaparaju JV, Mishra KA, Konrad N, Adamson J, Borovkov V, Aav R. Šakarašvili M, et al. Molecules. 2022 Jan 29;27(3):937. doi: 10.3390/molecules27030937. Molecules. 2022. PMID: 35164200 Free PMC article.
In order to investigate the ability of bis(zinc octaethylporphyrin) (bis-ZnOEP) to discriminate cyclohexanohemicucurbit[n]urils (cycHC[n]) of different shapes and sizes, the self-assembly of barrel-shaped chiral cycHC[n] with bis-ZnOEP was studied by v …
In order to investigate the ability of bis(zinc octaethylporphyrin) (bis-ZnOEP) to discriminate cyclohexanohemicucurbit[n]urils (cycH …
Synthesis of C-N Axially Chiral N-Arylbenzo[g]indoles via a Central-to-Axial Chirality Conversion Strategy.
Sun Y, Sun L, Zhang S, Zhang Z, Wang T. Sun Y, et al. Org Lett. 2024 May 23. doi: 10.1021/acs.orglett.4c01576. Online ahead of print. Org Lett. 2024. PMID: 38780223
Gold-catalyzed cascade cyclization of diynes for the synthesis of previously unexplored C-N axially chiral N-arylbenzo[g]indoles was described. The transformation was achieved via a central-to-axial chirality conversion strategy. The chiral conv …
Gold-catalyzed cascade cyclization of diynes for the synthesis of previously unexplored C-N axially chiral N-arylbenzo[ …
Configurationally Chiral SuFEx-Based Polymers.
Liang DD, Pujari SP, Subramaniam M, Besten M, Zuilhof H. Liang DD, et al. Angew Chem Int Ed Engl. 2022 Feb 14;61(8):e202116158. doi: 10.1002/anie.202116158. Epub 2022 Jan 11. Angew Chem Int Ed Engl. 2022. PMID: 34919320 Free PMC article.
The enantiospecific sulfur-fluorine exchange (SuFEx) reaction of chiral di-sulfonimidoyl fluorides (di-SFs) with diphenols, was used to produce high-molecular-weight chiral polymers with configurational backbone chirality. The resulting new class of polymers, …
The enantiospecific sulfur-fluorine exchange (SuFEx) reaction of chiral di-sulfonimidoyl fluorides (di-SFs) with diphenols, was used …
Asymmetric synthesis of N-N axially chiral compounds via organocatalytic atroposelective N-acylation.
Lin W, Zhao Q, Li Y, Pan M, Yang C, Yang GH, Li X. Lin W, et al. Chem Sci. 2021 Nov 24;13(1):141-148. doi: 10.1039/d1sc05360d. eCollection 2021 Dec 22. Chem Sci. 2021. PMID: 35059162 Free PMC article.
Compared with the well-developed C-C and C-N axial chirality, the asymmetric synthesis of N-N axial chirality remains elusive and challenging. ...This reaction features mild conditions and a broad substrate scope and produces N-N a …
Compared with the well-developed C-C and C-N axial chirality, the asymmetric synthesis of N-N axial chirality
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