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Books on the topic 'Rearrangements (Chemistry) Chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Polar rearrangements. Oxford University Press, 1992.

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2

Patel, Sunita Thakordas. Sigmatropic rearrangements in organofluorine chemistry. University of Birmingham, 1994.

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3

Plath, Peter Jörg. Diskrete Physik molekularer Umlagerungen. Teubner, 1988.

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4

Molecular rearrangements in organic synthesis. John Wiley & Sons, Inc., 2015.

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5

Lin, Zhi-Ping. Some applications of ultrasound irradiation in pinacol coupling of carbonyl compounds. Nova Science Publishers, 2010.

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6

Baer, Tomas. Unimolecular reaction dynamics: Theory and experiments. Oxford University Press, 1996.

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7

Anisimov, A. V. Molekuli͡a︡rnye peregruppirovki seroorganicheskikh soedineniĭ: Organicheskie sulʹfidy. Izd-vo Moskovskogo universiteta, 1989.

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8

Witczak, Zbigniew J., and Roman Bielski. Domino and intramolecular rearrangement reactions as advanced synthetic methods in glycoscience. John Wiley & Sons Inc., 2016.

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9

Photoisomerization: Causes, Behavior and Effects. Nova Science Publishers, Incorporated, 2019.

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10

Daruwala, Khushroo Peshotan. Substituent control in the oxy-Cope rearrangements of 1-vinyl-trans-cyclotridec-3-en-1-ol systems. 1986.

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11

Stütz, Arnold E. Glycoscience: Epimerisation, Isomerisation and Rearrangement Reactions of Carbohydrates (Topics in Current Chemistry) (Topics in Current Chemistry). Springer Verlag, 2001.

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12

SulfurMediated Rearrangements II Topics in Current Chemistry. Springer, 2010.

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13

Shahzad, Sohail Anjum. Novel Selenium-Mediated Rearrangements and Cyclisations. Springer, 2012.

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14

Shahzad, Sohail Anjum. Novel Selenium-Mediated Rearrangements and Cyclisations. Springer, 2012.

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15

Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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16

Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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17

Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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18

Zhang, Minghui. Model studies of coenzyme B₁₂-dependent rearrangements. 1993.

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19

BORODKIN, G. I., and V. G. Shubin. Molecular Rearrangements of Cationic Organic Complexes (Chemistry Reviews). Taylor & Francis, 2000.

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20

Keaffaber, Jeffrey J. Thermal rearrangements of bicyclic gem-dihalocyclopropanes: The aromatization of 6,6-difluorobicyclo(3.1.0)hex-2-ene and 2,3-benzo-6,6-dihalobicyclo(3.1.0)hex-2-ene derivatives. 1989.

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21

E, Stütz Arnold, ed. Glycoscience: Epimerisation, isomerisation and rearrangement reactions of carbohydrates. Springer, 2001.

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22

Deshayes, Kurt D. Studies of spiro[pyranindoline] compounds and their application to photodynamic transport. 1988.

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23

Conti, Nicholas Joseph. Thermal and photo-induced rearrangements of sigma-bound cyclopropyl iron complexes: Synthesis of a novel metallacyclic iron dicarbene complex. 1987.

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24

Phanstiel, Otto. The effect of a single fluorine substituent on the [1,5] homodienyl hydrogen shift, the solvolytic ring-opening of bromocyclopropane, and the [1,3] carbon shift of 6-methylenebicyclo[3.2.0]hept-2-ene. 1988.

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25

Wempe, Michael F. The transannular rearrangement of 5-cyclodecynone. 1993.

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26

Hiersemann, Martin, and Udo Nubbemeyer. Claisen Rearrangement: Methods and Applications. Wiley & Sons, Incorporated, John, 2007.

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27

Hiersemann, Martin, and Udo Nubbemeyer. Claisen Rearrangement: Methods and Applications. Wiley & Sons, Limited, John, 2007.

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28

Sulfur-Mediated Rearrangement II. Springer, 2007.

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29

Martin, Hiersemann, and Nubbemeyer Udo, eds. The Claisen rearrangement: Methods and applications. Wiley-VCH, 2007.

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30

Witczak, Zbigniew J., and Roman Bielski. Domino and Intramolecular Rearrangement Reactions As Advanced Synthetic Methods in Glycoscience. Wiley & Sons, Incorporated, John, 2016.

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31

Witczak, Zbigniew J., and Roman Bielski. Domino and Intramolecular Rearrangement Reactions As Advanced Synthetic Methods in Glycoscience. Wiley & Sons, Incorporated, John, 2016.

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32

Wempe, Michael F. The experimental and theoretical study of the acid catalyzed transannular rearrangement of 5-cyclodecynone to Bicyclo[4.4.0]-1(6)-decen-2-one. 1996.

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