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Refined by: Journal Title: Tetrahedron Letters remove
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1
A model approach towards the polycyclic framework present in cembranoid natural products dissectolide A, plumarellide and mandapamate
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A model approach towards the polycyclic framework present in cembranoid natural products dissectolide A, plumarellide and mandapamate

Tetrahedron Letters, 2014, Vol.55 (51), p.7068-7071 [Peer Reviewed Journal]

ISSN: 0040-4039 ;EISSN: 1873-3581

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2
Recent advances in the chemistry of 1,2,4-triazoles: Synthesis, reactivity and biological activities
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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

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3
Synthesis, characterisation and cytotoxic activity evaluation of new metal-salen complexes based on the 1,2-bicyclo[2.2.2]octane bridge
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Synthesis, characterisation and cytotoxic activity evaluation of new metal-salen complexes based on the 1,2-bicyclo[2.2.2]octane bridge

Tetrahedron letters, 2021-01, Vol.63 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2020.152706

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4
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
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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

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5
Efficient and multi-function compatible click-reaction of organosilanes
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Article
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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

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6
An attempt to synthesize the two monomers of CDTOH: Unexpected NMR and X-ray diffraction crystal analysis
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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

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7
Triphenylene: A versatile molecular receptor
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Triphenylene: A versatile molecular receptor

Tetrahedron letters, 2019-03, Vol.60, p.872-884 [Peer Reviewed Journal]

Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.02.033

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8
Graphene quantum dots: Emerging organic materials with remarkable and tunable luminescence features
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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

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9
Easy and efficient selenocyanation of imidazoheterocycles using triselenodicyanide
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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

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10
Diastereoselective ring cleavage of azetidines with cyanogen bromide
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Article
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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

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11
Regiocontrolled palladium-catalyzed direct C2-arylations of Methoxalen using benzenesulfonyl chlorides and C2,C3-diarylations using aryl bromides as the aryl sources
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Article
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Regiocontrolled palladium-catalyzed direct C2-arylations of Methoxalen using benzenesulfonyl chlorides and C2,C3-diarylations using aryl bromides as the aryl sources

Tetrahedron letters, 2020-01, Vol.61 (1) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.151342

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12
Synthesis of novel 3-(quinazol-2-yl)-quinolines via SNAr and aluminum chloride-induced (hetero) arylation reactions and biological evaluation as proteasome inhibitors
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Synthesis of novel 3-(quinazol-2-yl)-quinolines via SNAr and aluminum chloride-induced (hetero) arylation reactions and biological evaluation as proteasome inhibitors

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.2020.151805

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13
Synthesis and antibacterial activity of racemic paecilocin A and its derivatives against methicillin-sensitive and -resistant Staphylococcus aureus
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Article
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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

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14
General methodology for the chemoselective N-alkylation of (2,2,6,6)-tetramethylpiperidin-4-ol: Contribution of microwave irradiation
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General methodology for the chemoselective N-alkylation of (2,2,6,6)-tetramethylpiperidin-4-ol: Contribution of microwave irradiation

Tetrahedron letters, 2019-01, Vol.60 (3), p.240-243 [Peer Reviewed Journal]

Attribution - NonCommercial - NoDerivatives ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2018.12.020

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15
New D-π-A-conjugated organic sensitizers based on α-pyranylidene donors for dye-sensitized solar cells
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Article
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New D-π-A-conjugated organic sensitizers based on α-pyranylidene donors for dye-sensitized solar cells

Tetrahedron letters, 2017-03, Vol.58 (10), p.995-999 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2017.01.094

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16
Synthesis of N-pyrimidin[1,3,4]oxadiazoles and N-pyrimidin[1,3,4]-thiadiazoles from 1,3,4-oxadiazol-2-amines and 1,3,4-thiadiazol-2-amines via Pd-catalyzed heteroarylamination
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Synthesis of N-pyrimidin[1,3,4]oxadiazoles and N-pyrimidin[1,3,4]-thiadiazoles from 1,3,4-oxadiazol-2-amines and 1,3,4-thiadiazol-2-amines via Pd-catalyzed heteroarylamination

Tetrahedron letters, 2019-05, Vol.60 (20), p.1359-1362 [Peer Reviewed Journal]

Attribution - NonCommercial ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2019.04.022

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17
New triterpenoid saponins from the stem bark of Hallea ledermannii
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Article
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New triterpenoid saponins from the stem bark of Hallea ledermannii

Tetrahedron letters, 2023-02 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/j.tetlet.2022.154335

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18
New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
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New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation

Tetrahedron letters, 1998-05, Vol.39 (19), p.2941-2944 [Peer Reviewed Journal]

1998 ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/S0040-4039(98)00504-8

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19
Synthesis of indoles through acceptorless dehydrogenative coupling catalyzed by nickel on silica-alumina
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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

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20
Reactivity of antipyrine and haloantipyrines in Pd-catalyzed C–H bond arylations
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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

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