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1	Material Type: Article	Recent advances in the chemistry of 1,2,4-triazoles: Synthesis, reactivity and biological activities Tetrahedron letters, 2021-12, Vol.86 [Peer Reviewed Journal] Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153518 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	Designing photoswitches for molecular solar thermal energy storage Tetrahedron letters, 2015-03, Vol.56 (2015), p.1457 [Peer Reviewed Journal] ISSN: 1873-3581 ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2015.01.187 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	Graphene quantum dots: Emerging organic materials with remarkable and tunable luminescence features Tetrahedron letters, 2020-12, Vol.61 (49) [Peer Reviewed Journal] Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.152554 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Easy and efficient selenocyanation of imidazoheterocycles using triselenodicyanide Tetrahedron letters, 2017-07, Vol.58 (28), p.2771-2773 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2017.06.003 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Diastereoselective ring cleavage of azetidines with cyanogen bromide Tetrahedron letters, 2022-03, Vol.94 [Peer Reviewed Journal] Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2022.153710 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	Synthesis and antibacterial activity of racemic paecilocin A and its derivatives against methicillin-sensitive and -resistant Staphylococcus aureus Tetrahedron letters, 2021-03, Vol.67 [Peer Reviewed Journal] Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.152888 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	Multi-Component Reaction for the Preparation of 1,5-Disubstituted 1,2,3-Triazoles by In-Situ Generation of Azides and Nickel-Catalyzed Azide-Alkyne Cycloaddition Tetrahedron letters, 2021-06 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153131 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	Efficient and multi-function compatible click-reaction of organosilanes Tetrahedron letters, 2020-07, Vol.61 (30) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.152145 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Synthesis of indoles through acceptorless dehydrogenative coupling catalyzed by nickel on silica-alumina Tetrahedron letters, 2021-08, Vol.78 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153270 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
10	$An attempt to synthesize the two monomers of CDTOH: Unexpected NMR and X-ray diffraction crystal analysis$ $An attempt to synthesize the two monomers of CDTOH: Unexpected NMR and X-ray diffraction crystal analysis$ Material Type: Article	An attempt to synthesize the two monomers of CDTOH: Unexpected NMR and X-ray diffraction crystal analysis Tetrahedron letters, 2022-02, Vol.91 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2022.153638 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
11	Material Type: Article	Reactivity of antipyrine and haloantipyrines in Pd-catalyzed C–H bond arylations Tetrahedron letters, 2020-04, Vol.61 (17) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.151798 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	Versatile and base-free copper-catalyzed α-arylations of aromatic ketones using diaryliodonium salts Tetrahedron letters, 2021-07, Vol.75 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153208 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	Material Type: Article	Regiocontrolled palladium-catalyzed direct C2-arylation of a difluorobenzo[d]imidazole Tetrahedron letters, 2021-06, Vol.73 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153112 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
14	Material Type: Article	Regioselective 1,6-conjugate addition of organocuprate reagents to gamma-alkylidenebutenolides Tetrahedron letters, 2020-02, Vol.61 (6) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.151472 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	New synthetic route to 2,2,6,6-tetraethylpiperidin-4-one: A key-intermediate towards tetraethyl nitroxides Tetrahedron letters, 2019-10, Vol.60 (44) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.151207 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	Cobalt-catalyzed versus uncatalyzed intramolecular Diels-Alder cycloadditions Tetrahedron letters, 2018-01, Vol.59 (2), p.103-107 [Peer Reviewed Journal] Attribution - NonCommercial - NoDerivatives ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2017.11.052 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
17	Material Type: Article	A DMAP-catalyzed mild and efficient synthesis of 1,2-dihydroquinazolines via a one-pot three-component protocol Tetrahedron letters, 2014, Vol.55 (1), p.200-204 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2013.10.157 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	2- and 4-Nitrobenzenesulfonamides: Exceptionally versatile means for preparation of secondary amines and protection of amines Tetrahedron letters, 1995-09, Vol.36 (36), p.6373-6374 [Peer Reviewed Journal] 1995 ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/0040-4039(95)01316-A Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	A Passerini/Tsuji-Trost access to dienamide derivatives Tetrahedron letters, 2019-01, Vol.60 (2), p.102-105 [Peer Reviewed Journal] Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2018.11.068 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	Quest for novel fluorogenic xanthene dyes: Synthesis, spectral properties and stability of 3-imino-3H-xanthen-6-amine (pyronin) and its silicon analog Tetrahedron letters, 2018-12, Vol.59 (52), p.4574-4581 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2018.11.031 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by

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Results 1 - 20 of 24,891 for All Library Resources

Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153518

ISSN: 1873-3581 ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2015.01.187

Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.152554

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2017.06.003

Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2022.153710

Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.152888

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153131

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.152145

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153270

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2022.153638

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.151798

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153208

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2021.153112

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.151472

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.151207

Attribution - NonCommercial - NoDerivatives ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2017.11.052

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2013.10.157

1995 ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/0040-4039(95)01316-A

Copyright ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2018.11.068

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2018.11.031

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