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Books on the topic 'Cyclopropane'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 July 2024

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1

Boche, G. Cyclopropane derived reactive intermediates. Chichester: Wiley, 1990.

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2

Boche, Gernot. Cyclopropane derived reactive intermediates. Chichester: Wiley, 1990.

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3

Boche, G., and H. M. Walborsky, eds. Cyclopropane Derived Reactive Intermediates (1990). Chichester, UK: John Wiley & Sons, Inc., 1990. http://dx.doi.org/10.1002/9780470772409.

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4

A, Svi͡a︡tkin V., and Nefedov O. M, eds. Stroenie proizvodnykh t͡s︡iklopropana. Moskva: "Nauka", 1986.

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5

Rush, Stephen Howard. Palladium(II)-catalysed polymerisation of 3,3-disubtituted cyclopropenes. Dublin: University College Dublin, 1996.

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6

Kulinkovich, Oleg G. Cyclopropanes in organic synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015.

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7

Zvi, Rappoport, ed. The chemistry of the cyclopropyl group. Chichester: Wiley, 1987.

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8

Zvi, Rappoport, ed. The Chemistry of the cyclopropyl group. Chichester: Wiley, 1995.

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9

Netherlands. Werkgroep van Deskundigen ter Vaststelling van MAC-Waarden. Enflurane, isoflurane, and cyclopropane: Health based recommended occupational exposure limits : report of the Dutch Expert Committee on Occupational Standards, a committee of the Health Council of the Netherlands. Den Haag: Health Council of the Netherlands, 1998.

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10

Kulinkovich, Oleg G. Cyclopropanes in Organic Synthesis. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118978429.

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11

1938-, McKervey M. Anthony, and Ye Tao 1963-, eds. Modern catalytic methods for organic synthesis with diazo compounds: From cyclopropanes to ylides. New York: Wiley, 1998.

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12

Rappoport, Zvi, G. Boche, Saul Patai, and H. M. Walborsky. Cyclopropane Derived Reactive Intermediates: Updates from the Chemistry of Functional Groups. Wiley & Sons, Limited, John, 2010.

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13

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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14

Kulinkovich, Oleg G. Cyclopropanes in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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15

Kulinkovich, Oleg G. Cyclopropanes in Organic Synthesis. Wiley & Sons, Limited, John, 2015.

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16

Kulinkovich, Oleg G. Cyclopropanes in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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17

Simon, Reyna Joy. The stereochemistry of the vinylcyclopropane rearrangement of trans-2-methyl-(trans-styryl)cyclopropane. 1987.

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18

Crowther, Donna Jean. Ring-opening reactions of cyclopropyl and cyclobutyl complexes of manganese and iron. 1989.

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19

Rappoport, Zvi. The Chemistry of the Cyclopropyl Group Volume 2 (Chemistry of Functional Groups). Wiley, 1996.

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20

Jia, Zhaozhong. Studies and Synthetic Applications of the O-stannyl Ketyl-promoted Cyclopropane Fragmentations. Dissertation Discovery Company, 2019.

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21

Jia, Zhaozhong. Studies and Synthetic Applications of the o-Stannyl Ketyl-promoted Cyclopropane Fragmentations. Creative Media Partners, LLC, 2019.

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22

Chemical Transformations of Vinylidenecyclopropanes. Springer, 2012.

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23

Chemical Transformations Of Vinylidenecyclopropanes. Springer, 2012.

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24

Shi, Min, Lixiong Shao, and Jianmei Lu. Chemical Transformations of Vinylidenecyclopropanes. Springer, 2012.

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25

Beck, Horace. Organic Chemistry Notebook: Hexagonal Graph Paper Notebook for Drawing Chemistry Structures, Chemistry Nerd Gift Cyclopropane, Organic, Joke. Independently Published, 2020.

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26

Overman, Larry E. Organic Reactions, Volume 58. Wiley, 2001.

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27

Novikov, Roman, Denis Borisov, Leonid Menchikov, and Yuriy Tomilov. Donor-acceptor cyclopropanes. Cycloaddition and annulation reactions. LCC MAKS Press, 2022. http://dx.doi.org/10.29003/m2659.978-5-317-06797-7.

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Abstract:

This is the second book in the Donor-Acceptor Cyclopropanes series. It summarizes and analyzes for the first time the main intermediates formed from D-A cyclopropanes, and also systematizes the main ways of their further transformations. The main attention is paid to the cycloaddition and annulation reactions of D-A cyclopropanes with various substrates under the action of Lewis acids, which are of the greatest practical importance in organic synthesis. The monograph is addressed to a wide range of specialists in the field of small cycle chemistry and organic synthesis, including the synthesis of natural compounds and biologically active substances

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28

Banerjee, Prabal, and Akkattu T. Biju. Donor-Acceptor Cyclopropanes in Organic Synthesis. Wiley & Sons, Incorporated, John, 2022.

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29

Banerjee, Prabal, and Akkattu T. Biju. Donor-Acceptor Cyclopropanes in Organic Synthesis. Wiley & Sons, Limited, John, 2022.

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30

Banerjee, Prabal, and Akkattu T. Biju. Donor-Acceptor Cyclopropanes in Organic Synthesis. Wiley & Sons, Incorporated, John, 2022.

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31

Banerjee, Prabal, and Akkattu T. Biju. Donor-Acceptor Cyclopropanes in Organic Synthesis. Wiley & Sons, Incorporated, John, 2022.

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32

Reiner, Stefan. Analoga der Cholinomimetika Arecolin und Isoarecolin. Derivate von Hexahydro-1H-cyclopropa[C]pyridincarbonsäuren und von 3-alkyl-1,2,3,6-tetrahydropyridin-3-carbonsäuren. Stuttgart, 1991.

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