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Journal articles on the topic 'Mn-catalyzed'

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Author: Grafiati
Published: 11 March 2023

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1

WHELAN, GENE, and RONALD C. SIMS. "Mn-Catalyzed Oxidation of Naphthalenediol." Hazardous Waste and Hazardous Materials 12, no. 4 (January 1995): 381–94. http://dx.doi.org/10.1089/hwm.1995.12.381.

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2

Nishikori, Hisashi, and Tsutomu Katsuki. "Mn-salen catalyzed enantioselective sulfimidation." Applied Catalysis A: General 194-195 (March 2000): 475–77. http://dx.doi.org/10.1016/s0926-860x(99)00393-2.

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3

Chen, Yuanjin, Tian Tian, and Zhiping Li. "Mn-Catalyzed azidation–peroxidation of alkenes." Organic Chemistry Frontiers 6, no. 5 (2019): 632–36. http://dx.doi.org/10.1039/c8qo01231h.

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4

Cozzi, P. "Mn-Catalyzed Reformatsky Reaction with Ketones." Synfacts 2006, no. 7 (June 2006): 0698. http://dx.doi.org/10.1055/s-2006-941862.

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5

Fu, Niankai, Yifan Shen, Anthony R. Allen, Lu Song, Atsushi Ozaki, and Song Lin. "Mn-Catalyzed Electrochemical Chloroalkylation of Alkenes." ACS Catalysis 9, no. 1 (December 5, 2018): 746–54. http://dx.doi.org/10.1021/acscatal.8b03209.

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6

Rehman, S., M. Hafeez, U. Manzoor, M. A. Khan, and A. S. Bhatti. "Competitive role of Mn diffusion with growth in Mn catalyzed nanostructures." Journal of Applied Physics 111, no. 8 (April 15, 2012): 084301. http://dx.doi.org/10.1063/1.3702881.

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7

Osipova, Elena S., Ekaterina S. Gulyaeva, Nikolay V. Kireev, Sergey A. Kovalenko, Christian Bijani, Yves Canac, Dmitry A. Valyaev, Oleg A. Filippov, Natalia V. Belkova, and Elena S. Shubina. "Fac-to-mer isomerization triggers hydride transfer from Mn(i) complex fac-[(dppm)Mn(CO)3H]." Chemical Communications 58, no. 32 (2022): 5017–20. http://dx.doi.org/10.1039/d2cc00999d.

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8

Schmidt and Husted. "The Biochemical Properties of Manganese in Plants." Plants 8, no. 10 (September 27, 2019): 381. http://dx.doi.org/10.3390/plants8100381.

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Manganese (Mn) is an essential micronutrient with many functional roles in plant metabolism. Manganese acts as an activator and co-factor of hundreds of metalloenzymes in plants. Because of its ability to readily change oxidation state in biological systems, Mn plays and important role in a broad range of enzyme-catalyzed reactions, including redox reactions, phosphorylation, decarboxylation, and hydrolysis. Manganese(II) is the prevalent oxidation state of Mn in plants and exhibits fast ligand exchange kinetics, which means that Mn can often be substituted by other metal ions, such as Mg(II), which has similar ion characteristics and requirements to the ligand environment of the metal binding sites. Knowledge of the molecular mechanisms catalyzed by Mn and regulation of Mn insertion into the active site of Mn-dependent enzymes, in the presence of other metals, is gradually evolving. This review presents an overview of the chemistry and biochemistry of Mn in plants, including an updated list of known Mn-dependent enzymes, together with enzymes where Mn has been shown to exchange with other metal ions. Furthermore, the current knowledge of the structure and functional role of the three most well characterized Mn-containing metalloenzymes in plants; the oxygen evolving complex of photosystem II, Mn superoxide dismutase, and oxalate oxidase is summarized.
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9

Zhang, Liang, Shuya Liu, Zhiguo Zhao, Hongmei Su, Jingcheng Hao, and Yao Wang. "(Salen)Mn(iii)-catalyzed chemoselective acylazidation of olefins." Chemical Science 9, no. 28 (2018): 6085–90. http://dx.doi.org/10.1039/c8sc01882k.

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10

Wang, Congyang, and Ting Liu. "Manganese-Catalyzed C(sp2)–H Addition to Polar Unsaturated Bonds." Synlett 32, no. 13 (March 27, 2021): 1323–29. http://dx.doi.org/10.1055/a-1468-6136.

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AbstractTransition-metal-catalyzed nucleophilic C–H addition of hydrocarbons to polar unsaturated bonds could intrinsically avoid prefunctionalization of substrates and formation of waste byproducts, thus featuring high step- and atom-economy. As the third most abundant transition metal, manganese-catalyzed C–H addition to polar unsaturated bonds remains challenging, partially due to the difficulty in building a closed catalytic cycle of manganese. In the past few years, we have developed manganese catalysis to enable the sp2-hydrid C–H addition to polar unsaturated bonds (e.g., imines, aldehydes, nitriles), which will be discussed in this personal account.1 Introduction2 Mn-Catalyzed N-Directed C(sp2)–H Addition to Polar Unsaturated Bonds3 Mn-Catalyzed O-Directed C(sp2)–H Addition to Polar Unsaturated Bonds4 Conclusion
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11

Ge, Luo, and Syuzanna R. Harutyunyan. "Manganese(i)-catalyzed access to 1,2-bisphosphine ligands." Chemical Science 13, no. 5 (2022): 1307–12. http://dx.doi.org/10.1039/d1sc06694c.

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Chiral bisphosphine ligands are of key importance in transition-metal-catalyzed asymmetric synthesis of optically active products. Mn(i)-catalyzed hydrophosphination offers a two-step, one-pot synthetic sequence to access chiral 1,2-bisphosphines.
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12

Attiogbe, Francis K., and Raymond C. Francis. "Hydrogen peroxide decomposition in bicarbonate solution catalyzed by divalent manganese species*This article has a companion paper in this issue (doi: 10.1139/v11-078)." Canadian Journal of Chemistry 89, no. 10 (October 2011): 1297–303. http://dx.doi.org/10.1139/v11-080.

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The peroxymonocarbonate mono- and di-anions (HCO4– and CO42–) are known to be generated from H2O2/HCO3–. They are promising oxidants for wood pulp bleaching, but peroxide decomposition catalyzed by Mn(II) species may be significant for pulp samples with unusually high Mn contents. This investigation aimed to see if HCO3– addition caused destabilization of the peroxygen system owing to its partial conversion to HCO4–. This anionic peracid is a much stronger oxidant than H2O2 and could lead to a higher rate of Mn(II) oxidation to Mn(III) and (or) Mn(IV). For most free radical chain mechanisms, an increase in Mn(II) oxidation results in a higher rate of peroxide decomposition. Peroxide decomposition catalyzed by Mn(II) was investigated in H2O2/HCO3 in the pH ranges 8.5–8.7 and 7.4–7.9. The rate equation for peroxide decomposition was first order in [H2O2] and [Mn(II)] in both pH ranges, but close to second order in [HCO3–] in the higher pH range and close to third order in the lower pH range. Free radical chain mechanisms were proposed for both pH ranges and with all the correct reaction orders. Contrary to mechanisms previously proposed, it was concluded that HCO4– is the principal oxidizer of Mn(II) in the pH 7.4–7.9 range.
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13

WHELAN, GENE, and RONALD C. SIMS. "Mn-Catalyzed Oxidation of Multiple-Ringed Aromatics." Hazardous Waste and Hazardous Materials 12, no. 3 (January 1995): 243–56. http://dx.doi.org/10.1089/hwm.1995.12.243.

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14

Gong, Hang, Juan Ma, and Jingyu Zhang. "Mn(II)-Catalyzed N-Acylation of Amines." Synthesis 51, no. 03 (September 4, 2018): 693–703. http://dx.doi.org/10.1055/s-0037-1610267.

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A practical protocol has been developed here for the Mn(II)-catalyzed N-acylation of amines with high yields using N,N-dimethylformamide and other amides as the carbonyl source. The protocol is simple, does not require any acid, base, ligand, or other additives, and encompasses a broad substrate scope for primary, secondary, and heterocyclic amines.
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15

Kohmura, Yoshinori, and Tsutomu Katsuki. "Mn(salen)-catalyzed enantioselective CH amination." Tetrahedron Letters 42, no. 19 (May 2001): 3339–42. http://dx.doi.org/10.1016/s0040-4039(01)00427-0.

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16

Fang, Yuan, Yonghui Wang, Fen Wang, Chengyong Shu, Jianfeng Zhu, and Wenling Wu. "Fe–Mn bimetallic oxides-catalyzed oxygen reduction reaction in alkaline direct methanol fuel cells." RSC Advances 8, no. 16 (2018): 8678–87. http://dx.doi.org/10.1039/c7ra12610g.

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Heterojunction interfaces and synergistic effect between Fe2O3 and Mn2O3 play a key role in Fe2O3/Mn2O3-catalyzed ORR.
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17

Wen, Zhengcheng, Mengmeng Du, Yuan Li, Zhihua Wang, Jiangrong Xu, and Kefa Cen. "Quantum chemistry study on the oxidation of NO catalyzed by ZSM5 supported Mn/Co–Al/Ce." Journal of Theoretical and Computational Chemistry 16, no. 05 (August 2017): 1750044. http://dx.doi.org/10.1142/s0219633617500444.

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The detailed mechanism of NO oxidation catalyzed by ZSM5 supported Mn/Co–Al/Ce is investigated and revealed by Quantum Chemistry Calculation. A three-step catalytic mechanism for NO oxidation is proposed and studied. Theoretical results show that, the activate energies of reactions catalyzed by ZSM-5 supported Mn/Co (71.1[Formula: see text]kJ/mol/80.6[Formula: see text]kJ/mol) are much lower than that obtained from the direct NO oxidation. This indicates that the ZSM-5 supported Mn/Co has an obvious catalytic effect. When the active center Si is replaced by Al and Ce, the activation energies are further decreased to about 40[Formula: see text]kJ/mol. This indicates that the doping of Al and Ce can obviously improve the catalytic effect. The theoretical study illustrates that the catalysts for NO oxidation not only relate to the supported transition metal such as Co and Mn, but also highly relate to the activity centers such as Al and Ce.
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18

Xie, Jin, Zhongfei Yan, and Chengjian Zhu. "Manganese(I)-Catalyzed Selective Functionalization of Alkynes." Synlett 30, no. 02 (November 30, 2018): 124–28. http://dx.doi.org/10.1055/s-0037-1610335.

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Mn(I)-catalyzed selective functionalization of alkynes permits the convenient synthesis of substituted alkenes with high step and atom economies. Although the insertion of five-membered chelated manganacycle intermediates into alkynes has been widely reported, nonchelated Ar–Mn(I) species originating from commercially available arylboronic acids are unprecedented. Our new protocol achieved a challenging hydroarylation of unsymmetrical 1,3-diynes with arylboronic acids with complete regio-, stereo-, and chemoselectivity to give a wide array of trisubstituted conjugated (Z)-enynes in moderate to good yields.
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19

Strekalova, S. O., M. N. Khrizanforov, T. V. Gryaznova, V. V. Khrizanforova, and Yu H. Budnikova. "Electrochemical phosphorylation of coumarins catalyzed by transition metal complexes (Ni—Mn, Co—Mn)." Russian Chemical Bulletin 65, no. 5 (May 2016): 1295–98. http://dx.doi.org/10.1007/s11172-016-1451-7.

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20

Goto, Atsushi, Koji Nagasawa, Ayaka Shinjo, Yoshinobu Tsujii, and Takeshi Fukuda. "Reversible Chain Transfer Catalyzed Polymerization of Methyl Methacrylate with In-Situ Formed Alkyl Iodide Initiator." Australian Journal of Chemistry 62, no. 11 (2009): 1492. http://dx.doi.org/10.1071/ch09229.

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A method utilizing generation of an alkyl iodide (low-mass dormant species) in situ formed in polymerization was adopted to reversible chain transfer catalyzed polymerizations (RTCP) (living radical polymerizations) with several nitrogen and phosphorus catalysts. The polymerization of methyl methacrylate afforded low-polydispersity polymers (Mw/Mn ~1.2–1.4), with Mn values predicted to high conversions; where Mn and Mw are the number- and weight-average molecular weights respectively. This method is robust and would enhance the utility of RTCP.
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21

Yang, Bobin, Wei Yao, Xiao-Feng Xia, and Dawei Wang. "Mn-Catalyzed 1,6-conjugate addition/aromatization of para-quinone methides." Organic & Biomolecular Chemistry 16, no. 24 (2018): 4547–57. http://dx.doi.org/10.1039/c8ob01057a.

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22

Nogi, Keisuke, Tetsuaki Fujihara, Jun Terao, and Yasushi Tsuji. "Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide." Chem. Commun. 50, no. 86 (2014): 13052–55. http://dx.doi.org/10.1039/c4cc03644a.

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23

Shao, Zhihui, Yujie Wang, Yaqian Liu, Qian Wang, Xiaoling Fu, and Qiang Liu. "A general and efficient Mn-catalyzed acceptorless dehydrogenative coupling of alcohols with hydroxides into carboxylates." Organic Chemistry Frontiers 5, no. 8 (2018): 1248–56. http://dx.doi.org/10.1039/c8qo00023a.

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24

Wang, Juping, Kangcheng Zheng, Ting Li, and Xiaojing Zhan. "Mechanism and Chemoselectivity of Mn-Catalyzed Intramolecular Nitrene Transfer Reaction: C–H Amination vs. C=C Aziridination." Catalysts 10, no. 3 (March 4, 2020): 292. http://dx.doi.org/10.3390/catal10030292.

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The reactivity, mechanism and chemoselectivity of the Mn-catalyzed intramolecular C–H amination versus C=C aziridination of allylic substrate cis-4-hexenylsulfamate are investigated by BP86 density functional theory computations. Emphasis is placed on the origins of high reactivity and high chemoselectivity of Mn catalysis. The N p orbital character of frontier orbitals, a strong electron-withdrawing porphyrazine ligand and a poor π backbonding of high-valent MnIII metal to N atom lead to high electrophilic reactivity of Mn-nitrene. The calculated energy barrier of C–H amination is 9.9 kcal/mol lower than that of C=C aziridination, which indicates that Mn-based catalysis has an excellent level of chemoselectivity towards C–H amination, well consistent with the experimental the product ratio of amintion-to-aziridination I:A (i.e., (Insertion):(Aziridination)) >20:1. This extraordinary chemoselectivity towards C–H amination originates from the structural features of porphyrazine: a rigid ligand with the big π-conjugated bond. Electron-donating substituents can further increase Mn-catalyzed C–H amination reactivity. The controlling factors found in this work may be considered as design elements for an economical and environmentally friendly C–H amination system with high reactivity and high chemoselectivity.
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25

Long, Wenhao, Pengcheng Lian, Jingjing Li, and Xiaobing Wan. "Mn-Catalysed photoredox hydroxytrifluoromethylation of aliphatic alkenes using CF3SO2Na." Organic & Biomolecular Chemistry 18, no. 33 (2020): 6483–86. http://dx.doi.org/10.1039/d0ob01322f.

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26

Sharma, Rohit, Firdoos Ahmad Sofi, Preeti Rana, and Prasad V. Bharatam. "Bimetallic Cu–Mn B spinel oxide catalyzed oxidative synthesis of 1,2-disubstituted benzimidazoles from benzyl bromides." New Journal of Chemistry 43, no. 10 (2019): 4013–16. http://dx.doi.org/10.1039/c8nj05504a.

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27

Sun, Q. "Mn/MFI catalyzed reduction of NOx with alkanes." Applied Catalysis B: Environmental 42, no. 4 (June 10, 2003): 393–401. http://dx.doi.org/10.1016/s0926-3373(02)00278-3.

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28

Biswas, Achintesh Narayan, Purak Das, Sujit Kumar Kandar, Arunava Agarwala, Debkumar Bandyopadhyay, and Pinaki Bandyopadhyay. "Chiral Mn(III) salen catalyzed oxidation of hydrocarbons." Transition Metal Chemistry 35, no. 5 (April 22, 2010): 527–30. http://dx.doi.org/10.1007/s11243-010-9359-9.

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29

Tateiwa, Jun-ichi, Keiji Hashimoto, Takayoshi Yamauchi, and Sakae Uemura. "Cation-Exchanged Montmorillonite (Mn+-Mont)-Catalyzed Prins Reaction." Bulletin of the Chemical Society of Japan 69, no. 8 (August 1996): 2361–68. http://dx.doi.org/10.1246/bcsj.69.2361.

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30

Fukuda, Tsutomu, and Tsutomu Katsuki. "Mn-salen catalyzed asymmetric oxidation of enol derivatives." Tetrahedron Letters 37, no. 25 (June 1996): 4389–92. http://dx.doi.org/10.1016/0040-4039(96)00858-1.

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31

Riguet, Eric, Ingo Klement, Ch Kishan Reddy, Gérard Cahiez, and Paul Knochel. "New mixed metal (Mn/Cu) catalyzed stereoselective cyclizations." Tetrahedron Letters 37, no. 33 (August 1996): 5865–68. http://dx.doi.org/10.1016/0040-4039(96)01249-x.

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32

Golchoubian, Hamid, and Nesa Ghasemi. "Diphenylmethane Oxidation Catalyzed by Mononuclear Mn(III) Complexes." Journal of the Chinese Chemical Society 58, no. 4 (August 2011): 470–73. http://dx.doi.org/10.1002/jccs.201190008.

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33

Wei, Zhihong, Adiran de Aguirre, Kathrin Junge, Matthias Beller, and Haijun Jiao. "Exploring the mechanisms of aqueous methanol dehydrogenation catalyzed by defined PNP Mn and Re pincer complexes under base-free as well as strong base conditions." Catalysis Science & Technology 8, no. 14 (2018): 3649–65. http://dx.doi.org/10.1039/c8cy00746b.

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34

Xu, Daqian, Qiangsheng Sun, Jin Lin, and Wei Sun. "Ligand regulation for manganese-catalyzed enantioselective epoxidation of olefins without acid." Chemical Communications 56, no. 86 (2020): 13101–4. http://dx.doi.org/10.1039/d0cc04440g.

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35

Wang, Xiao-Yu, Yong-Qin He, Mei Wang, Yi Zhou, Na Li, Xian-Rong Song, Zhao-Zhao Zhou, Wan-Fa Tian, and Qiang Xiao. "Visible-light-driven proton reduction for semi-hydrogenation of alkynes via organophotoredox/manganese dual catalysis." RSC Advances 12, no. 55 (2022): 36138–41. http://dx.doi.org/10.1039/d2ra07920h.

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36

Wang, Yang, Xiaofeng Zhang, Haixiong Liu, Hui Chen, and Deguang Huang. "Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent." Organic Chemistry Frontiers 4, no. 1 (2017): 31–36. http://dx.doi.org/10.1039/c6qo00451b.

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37

Jones, C., S. A. Crowe, A. Sturm, K. L. Leslie, L. C. W. MacLean, S. Katsev, C. Henny, D. A. Fowle, and D. E. Canfield. "Biogeochemistry of manganese in ferruginous Lake Matano, Indonesia." Biogeosciences 8, no. 10 (October 26, 2011): 2977–91. http://dx.doi.org/10.5194/bg-8-2977-2011.

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Abstract. This study explores Mn biogeochemistry in a stratified, ferruginous lake, a modern analogue to ferruginous oceans. Intense Mn cycling occurs in the chemocline where Mn is recycled at least 15 times before sedimentation. The product of biologically catalyzed Mn oxidation in Lake Matano is birnessite. Although there is evidence for abiotic Mn reduction with Fe(II), Mn reduction likely occurs through a variety of pathways. The flux of Fe(II) is insufficient to balance the reduction of Mn at 125 m depth in the water column, and Mn reduction could be a significant contributor to CH4 oxidation. By combining results from synchrotron-based X-ray fluorescence and X-ray spectroscopy, extractions of sinking particles, and reaction transport modeling, we find the kinetics of Mn reduction in the lake's reducing waters are sufficiently rapid to preclude the deposition of Mn oxides from the water column to the sediments underlying ferruginous water. This has strong implications for the interpretation of the sedimentary Mn record.
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38

Shi, Lijun, Xiang Zhong, Houde She, Ziqiang Lei, and Fuwei Li. "Manganese catalyzed C–H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity." Chemical Communications 51, no. 33 (2015): 7136–39. http://dx.doi.org/10.1039/c5cc00249d.

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39

Zhang, Yaxing, Jianyu Dong, Lixin Liu, Long Liu, Yongbo Zhou, and Shuang-Feng Yin. "Manganese(iii) acetate catalyzed oxidative amination of benzylic C(sp3)–H bonds with nitriles." Organic & Biomolecular Chemistry 15, no. 14 (2017): 2897–901. http://dx.doi.org/10.1039/c7ob00512a.

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40

Ju, Yeming, Di Miao, Ruiyang Yu, and Sangho Koo. "Tandem catalytic oxidative deacetylation of acetoacetic esters and heteroaromatic cyclizations." Organic & Biomolecular Chemistry 13, no. 9 (2015): 2588–99. http://dx.doi.org/10.1039/c4ob02441a.

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41

Kong, Gui-Xian, Jiao-Na Han, Dandan Yang, Jun-Long Niu, and Mao-Ping Song. "Manganese-catalyzed cascade annulations of alkyne-tethered N-alkoxyamides: synthesis of polycyclic isoquinolin-1(2H)-ones." Organic & Biomolecular Chemistry 17, no. 48 (2019): 10167–71. http://dx.doi.org/10.1039/c9ob02364j.

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42

Castaman, Silvana T., Shirley Nakagaki, Ronny R. Ribeiro, Kátia J. Ciuffi, and Sueli M. Drechsel. "Homogeneous and heterogeneous olefin epoxidation catalyzed by a binuclear Mn(II)Mn(III) complex." Journal of Molecular Catalysis A: Chemical 300, no. 1-2 (March 2009): 89–97. http://dx.doi.org/10.1016/j.molcata.2008.10.037.

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43

Li, Qianqian, Suhong Huo, Lingpeng Meng, and Xiaoyan Li. "Mechanism and origin of the stereoselectivity of manganese-catalyzed hydrosilylation of alkynes: a DFT study." Catalysis Science & Technology 12, no. 8 (2022): 2649–58. http://dx.doi.org/10.1039/d1cy02340c.

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44

Liu, Bingxian, Yin Yuan, Panjie Hu, Guangfan Zheng, Dachang Bai, Junbiao Chang, and Xingwei Li. "Mn(i)-Catalyzed nucleophilic addition/ring expansion via C–H activation and C–C cleavage." Chemical Communications 55, no. 72 (2019): 10764–67. http://dx.doi.org/10.1039/c9cc05973c.

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45

Cembellín, Sara, Iván Maisuls, Constantin G. Daniliuc, Helena Osthues, Nikos L. Doltsinis, Cristian A. Strassert, and Frank Glorius. "One-step synthesis of indolizino[3,4,5-ab]isoindoles by manganese(i)-catalyzed C–H activation: structural studies and photophysical properties." Organic & Biomolecular Chemistry 20, no. 4 (2022): 796–800. http://dx.doi.org/10.1039/d1ob02246f.

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46

Herrero, Christian, Annamaria Quaranta, Rémy Ricoux, Alexandre Trehoux, Atif Mahammed, Zeev Gross, Frédéric Banse, and Jean-Pierre Mahy. "Oxidation catalysis via visible-light water activation of a [Ru(bpy)3]2+ chromophore BSA–metallocorrole couple." Dalton Transactions 45, no. 2 (2016): 706–10. http://dx.doi.org/10.1039/c5dt04158a.

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Light induced enantioselective oxidation of thioanisole with water as the oxygen atom source is catalyzed by a Mn-corrole–BSA artificial metalloenzyme in the presence of a photoactivable ruthenium complex.
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47

Hu, Yu-Lin, Dong Fang, and Rong Xing. "Efficient and convenient oxidation of sulfides to sulfoxides with molecular oxygen catalyzed by Mn(OAc)2 in ionic liquid [C12mim][NO3]." RSC Adv. 4, no. 93 (2014): 51140–45. http://dx.doi.org/10.1039/c4ra06695b.

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48

Hu, Xinyu, Bobin Yang, Wei Yao, and Dawei Wang. "Alanine Triazole Mn-Catalyzed Coupling/Aromatization of Quinone Methides." Chinese Journal of Organic Chemistry 38, no. 12 (2018): 3296. http://dx.doi.org/10.6023/cjoc201805019.

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49

Nishino, Hiroshi, and Md Aminul Haque. "Synthesis of Peroxylactones Using Mn(III)-Catalyzed Aerobic Oxidation." HETEROCYCLES 83, no. 8 (2011): 1783. http://dx.doi.org/10.3987/com-11-12241.

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50

Fukuda, Tsutomu, Ryo Irie, and Tsutomu Katsuki. "Mn-Salen Catalyzed Asymmetric Epoxidation of Conjugated Trisubstituted Olefins." Synlett 1995, no. 02 (February 1995): 197–98. http://dx.doi.org/10.1055/s-1995-4916.

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