Academic literature on the topic 'Thermal rearrangements'

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Journal articles on the topic "Thermal rearrangements"

1

Zeller, Klaus-Peter. "Thermal Rearrangements of Azulenes." Bulletin des Sociétés Chimiques Belges 91, no. 5 (2010): 444. http://dx.doi.org/10.1002/bscb.198209105103.

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2

Jarzȩcki, Andrzej A., Joseph Gajewski, and Ernest R. Davidson. "Thermal Rearrangements of Norcaradiene." Journal of the American Chemical Society 121, no. 29 (1999): 6928–35. http://dx.doi.org/10.1021/ja984471l.

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3

Platz, M. S., Haiyong Huang, Francis Ford, and J. Toscano. "Photochemical rearrangements of diazirines and thermal rearrangements of carbenes." Pure and Applied Chemistry 69, no. 4 (1997): 803–8. http://dx.doi.org/10.1351/pac199769040803.

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4

KAWANO, Motoharu, and Katsutoshi TOMITA. "Thermal rearrangements for dioctahedral smectite." Journal of the Mineralogical Society of Japan 19 (1990): 11–15. http://dx.doi.org/10.2465/gkk1952.19.special_11.

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5

Casara, Patrick. "Vigabatrin synthesis by thermal rearrangements." Tetrahedron Letters 35, no. 19 (1994): 3049–50. http://dx.doi.org/10.1016/s0040-4039(00)76824-9.

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6

Billups, W. E., and Robert E. Bachman. "The thermal rearrangements of halocyclopropenes." Tetrahedron Letters 33, no. 14 (1992): 1825–26. http://dx.doi.org/10.1016/s0040-4039(00)74152-9.

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7

Wladislaw, B., L. Marzorati, and F. C. Biaggio. "Novel uncatalyzed thermal Pummerer rearrangements." Journal of Organic Chemistry 58, no. 22 (1993): 6132–34. http://dx.doi.org/10.1021/jo00074a051.

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8

Larsson, F. C. V., L. Brandsma, and S. O. Lawesson. "Thermal rearrangements of divinyl disulfides." Recueil des Travaux Chimiques des Pays-Bas 93, no. 9-10 (2010): 258–60. http://dx.doi.org/10.1002/recl.19740930908.

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9

Brown, R. F. C. "Thermal rearrangements of alkynes under FVP conditions. the acetylene-methylenecarbene rearrangement." Recueil des Travaux Chimiques des Pays-Bas 107, no. 12 (2010): 655–61. http://dx.doi.org/10.1002/recl.19881071202.

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10

Harrowven, David, Wei Sun, and Dharyl Wilson. "Steric Buttressing Changes Torquospecificity in Thermal Cyclo­butenone Rearrangements, Providing New Opportunities for 5H-Furanone Synthesis." Synthesis 49, no. 14 (2017): 3091–106. http://dx.doi.org/10.1055/s-0036-1588850.

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Abstract:
Thermally induced rearrangements of 4-hydroxycyclo­butenones are known to provide clean and reliable access to an array of useful carbocyclic and fused heterocyclic ring systems. Rarely, such reactions have been diverted to an alternative pathway leading to furanone formation. Herein, we show that these switches in the course of the rearrangement occur when a substrate bears a bulky substituent and are due to adverse steric buttressing as the transition state for electrocyclisation is approached. We also show how the reaction provides new opportunities for furanone synthesis and how bulky prot
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