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1	Material Type: Book	The Saegusa Oxidation and Related Procedures Distributed under a Creative Commons Attribution 4.0 International License ;DOI: 10.1002/0471264180.or098.01 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	Use of ArSO 2 SR f reagents: an efficient tool for the introduction of SR f moieties Organic & biomolecular chemistry, 2019-02, Vol.17 (7), p.1683-1693 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/c8ob02995d Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	Selective Activation of Chalcogen Bonding: An Efficient Structuring Tool toward Crystal Engineering Strategies Accounts of chemical research, 2024-02, Vol.57 (3), p.362-374 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/acs.accounts.3c00674 ;PMID: 38275221 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Electronic Decoupling in C3-Symmetrical Light-Responsive Tris(Azobenzene) Scaffolds: Self-Assembly and Multiphotochromism Journal of the American Chemical Society, 2018-11, Vol.140 (47), p.16062-16070 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b06324 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Photochemical Ring-Opening Reaction of 1,3-Cyclohexadiene: Identifying the True Reactive State Journal of the American Chemical Society, 2022-12, Vol.144 (48), p.21878-21886 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.2c06296 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	Experimental and Theoretical Study of the Kinetics of the CH 3 + HBr → CH 4 + Br Reaction and the Temperature Dependence of the Activation Energy of CH 4 + Br → CH 3 + HBr The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2023-08, Vol.127 (33), p.6916-6923 [Peer Reviewed Journal] Attribution ;ISSN: 1089-5639 ;EISSN: 1520-5215 ;DOI: 10.1021/acs.jpca.3c03685 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	Chemistry of Strigolactones, Key Players in Plant Communication Chembiochem : a European journal of chemical biology, 2024-04 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1439-4227 ;EISSN: 1439-7633 ;DOI: 10.1002/cbic.202400133 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	An electrochemical access to 2-amino-2,3-dihydro-1,4-benzodioxanes derived from hydroxytyrosol Organic & biomolecular chemistry, 2024, Vol.22 (5), p.1057-1063 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob01858j Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis Journal of organic chemistry, 2022-05, Vol.87 (9), p.5690-5702 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c00054 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
10	Material Type: Article	Palladium catalysis: dependence of the C-C bond synthesis efficiency on carboxylate ligand and alkali metal carboxylate or carboxylic acid additive. Part A: the C(sp 2 )-C(sp 2 ), C(sp 2 )-C(sp 3 ) and C(sp 3 )-C(sp 3 ) bonds Advanced synthesis & catalysis, 2023-10, Vol.365 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.202300903 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
11	Material Type: Article	CO 2 Hydroboration: Impact of the Boryl Moieties on the Reactivity of Four Bis(boryl)acetal Compounds toward 2,6‐Diisopropylaniline European journal of organic chemistry, 2023-08, Vol.26 (30) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202300525 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	Remote Radical Trifluoromethylation: A Unified Approach to the Selective Synthesis of γ-Trifluoromethyl α,β-Unsaturated Carbonyl Compounds Organic letters, 2022-12, Vol.24 (51), p.9375-9380 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c03676 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	Material Type: Article	Improved slow magnetic relaxation in optically pure helicene-based Dy(III) single molecule magnets Chemical communications (Cambridge, England), 2016, Vol.52 (100), p.14474-14477 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/C6CC08638A ;PMID: 27904894 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
14	Material Type: Article	Tuning the Charge Transfer in lambda 5 -Phosphinines with Amino-substituents Organic letters, 2022-09, Vol.24 (37) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c02846 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	Recent Developments in Asymmetric Nazarov Reactions Current organic chemistry, 2024 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1385-2728 ;EISSN: 1875-5348 ;DOI: 10.2174/0113852728296619240321060646 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	From A 3 /KA 2 to AYA/KYA multicomponent coupling reactions with terminal ynamides as alkyne surrogates – a direct, green route to γ-amino-ynamides Green chemistry : an international journal and green chemistry resource : GC, 2022-08, Vol.24 (17), p.6467-6475 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1463-9262 ;EISSN: 1463-9270 ;DOI: 10.1039/D2GC00966H Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
17	Material Type: Article	Regio- and stereocontrolled synthesis of borylated E -enynes, Z -enediynes and derivatives from alkenyl-1,2-bis-(boronates) Organic & biomolecular chemistry, 2023, Vol.21 (37), p.7567-7571 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob00543g Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	Sonochemically‐Induced Reduction of Alkenes to Alkanes with Ammonnia Angewandte Chemie International Edition, 2022, Vol.61 (51) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.202212719 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	On the road for more efficient biocompatible two-photon excitable fluorophores Chemistry : a European journal, 2022-01 [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202104378 ;PMID: 35060213 Digital Resources/Online E-Resources View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	Lysosomal targeting of b-cyclodextrin Chemistry : a European journal, 2022, Vol.29 (4) [Peer Reviewed Journal] Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202203252 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 9,636 for All Library Resources

Distributed under a Creative Commons Attribution 4.0 International License ;DOI: 10.1002/0471264180.or098.01

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/c8ob02995d

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/acs.accounts.3c00674 ;PMID: 38275221

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.8b06324

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/jacs.2c06296

Attribution ;ISSN: 1089-5639 ;EISSN: 1520-5215 ;DOI: 10.1021/acs.jpca.3c03685

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1439-4227 ;EISSN: 1439-7633 ;DOI: 10.1002/cbic.202400133

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob01858j

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c00054

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.202300903

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202300525

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c03676

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/C6CC08638A ;PMID: 27904894

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c02846

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1385-2728 ;EISSN: 1875-5348 ;DOI: 10.2174/0113852728296619240321060646

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1463-9262 ;EISSN: 1463-9270 ;DOI: 10.1039/D2GC00966H

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob00543g

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.202212719

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202104378 ;PMID: 35060213

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202203252

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