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Cyclobutanes synthesis

Scheme 3.23. Cyclobutene and alkylidine cyclobutane synthesis by stannylcupration of alkynes and trapping of the resultant vinylcuprate with epoxides [15c],... Scheme 3.23. Cyclobutene and alkylidine cyclobutane synthesis by stannylcupration of alkynes and trapping of the resultant vinylcuprate with epoxides [15c],...
Mann G, Muchall HM (1997) Cyclobutanes synthesis by rearrangement of the carbon framework. In de Meijere A (ed) Methods of organic chemistry (Houben-Weyl), 4th edn, vol E 17e. Thieme Verlag, Stuttgart, p 233... [Pg.40]

Diels-Alder, imino dienophiles, 65, 2 Diels-Alder, intramolecular, 32, 1 Diels-Alder, maleic anhydride, 4, 1 [4 -h 3], 51, 3 of enones, 44, 2 of ketenes, 45, 2 of nitrones and alkenes, 36, 1 Pauson-Khand, 40, 1 photochemical, 44, 2 retro-Diels-Alder reaction, 52, 1 53, 2 [6-h4], 49, 2 [3-h2], 61, 1 Cyclobutanes, synthesis ... [Pg.587]

Cyclobutanes, synthesis (Continued) by thermal cycloaddition reactions, 12, 1... [Pg.588]

Kaupp G (1995) Cyclobutane synthesis in the solid phase. In Horspool WM (ed) CRC Handbook of organic photochemistry and photobiology. CRC, Boca Raton, chap 4... [Pg.183]

Cyclopropane derivatives, including spiropentanc, have proven to be virtually inert towards carbenes,1 For this reason, no literature report that describes cyclobutane synthesis from a C3 and a Cj building block by ring enlargement of cyclopropanes exists. However, due to the partial p character, as well as the increasing reactivity caused by its strain, the central bond of bicyclo[1.1.0]butane (l)2 has been found to react with carbenes.1 Photolysis of diazomethane in the presence of bicyclo[1.1.0]butane (1) at — 50 C provides a mixture of several compounds. The major fraction of the material (80%) was analyzed by means of NMR spectrometry and found to consist of penta-1,4-diene (2, 21%) and bicyclo[l.l.l]pentane (3, 1%), plus several other known compounds as well as some unidentified products.3 The mechanistic pathway for the formation of bicyclo[l.l.l]pentane (3) has not been addressed in detail, but it is believed that a diradical intermediate is involved, as shown below.3... [Pg.76]


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See also in sourсe #XX -- [ Pg.430 ]

See also in sourсe #XX -- [ Pg.430 ]

See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.430 ]

See also in sourсe #XX -- [ Pg.250 , Pg.251 , Pg.252 ]




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Asymmetric cyclobutane synthesis

Bicyclic cyclobutanes synthesis

Chiral cyclobutane synthesis

Cyclic compounds cyclobutanes, synthesis

Cyclization cyclobutane synthesis

Cyclization malonic ester synthesis of cyclobutane

Cycloaddition reaction cyclobutane synthesis and

Cycloaddition reactions cyclobutanes, synthesis

Cyclobutanation

Cyclobutane

Cyclobutane synthesis

Cyclobutane synthesis

Cyclobutanes

Cyclobutanes, 1,2-divinylCope rearrangement synthesis

Cyclobutanes, synthesis from photocycloaddition

Cyclobutanes, vinylrearrangements synthesis

Polycyclic cyclobutane derivatives, synthesis

Syntheses of Alkylidene cyclobutanes

Syntheses of Alkylidene cyclobutanes from 1-Alkyl-l-selenocyclobutanes

Tetracyclic cyclobutanes, synthesis,

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