Oxidation of dimethyldi(2-pyridyl)borato PtIIMen complexes, n = 1, 0, with H2O2: tandem B-to-Pt methyl group migration and formation of C–O bond

2012 ◽  
Vol 41 (26) ◽  
pp. 8116 ◽  
Author(s):  
Shrinwantu Pal ◽  
Andrei N. Vedernikov
Keyword(s):  
Methyl Group ◽  
Group Migration

Thujopsene rearrangements. Ring system via methyl group migration

1972 ◽  
Vol 37 (2) ◽  
pp. 241-250 ◽  
Author(s):  
W. G. Dauben ◽  
L. E. Friedrich
Keyword(s):  
Ring System ◽  
Methyl Group ◽  
Group Migration

Methyl group migration in the preparation of o-tolyl- and p-xylyldichloroboranes

1967 ◽  
Vol 6 (11) ◽  
pp. 1975-1977 ◽  
Author(s):  
C. A. Eggers ◽  
Sidney F. A. Kettle
Keyword(s):  
Methyl Group ◽  
Group Migration

Tetracyclic triterpenes. VIII. The skeletal rearrangement of 3β-acetoxy-9α,11α-epoxy-5α-lanostan-7-one: 13- and 10-methyl group migration

1985 ◽  
Vol 63 (6) ◽  
pp. 1280-1286 ◽  
Author(s):  
Zdzisław Paryzek ◽  
Roman Wydra
Keyword(s):  
Acetic Anhydride ◽  
Spectral Data ◽  
Boron Trifluoride ◽  
Boron Trifluoride Etherate ◽  
Major Product ◽  
Chemical Transformations ◽  
Skeletal Rearrangement ◽  
Methyl Group ◽  
Group Migration

The boron trifluoride etherate catalyzed rearrangement of 3β-acetoxy-9α, 11α-epoxy-5α-lanostan-7-one (1) in acetic anhydride resulted in formation of 19(10 → 9β)abeo compounds 2 and 4 along with 18(13 → 12β)abeo compound 5, as the major product. These structures are supported by spectral data and chemical transformations. The possible mechanism of the rearrangement is discussed.

scholarly journals An unexpected methyl group migration during on-column Stille derivatization of RNA

Tetrahedron ◽  
2014 ◽  
Vol 70 (2) ◽  
pp. 327-333 ◽  
Author(s):  
Lena Wicke ◽  
Joachim W. Engels
Keyword(s):  
Methyl Group ◽  
Group Migration

Synthesis of internally alkylated azuliporphyrins

2020 ◽  
Vol 24 (05n07) ◽  
pp. 817-829
Author(s):  
Julian S. D. Moriones ◽  
Alissa N. Latham ◽  
Timothy D. Lash
Keyword(s):  
Hydrochloric Acid ◽  
Alkyl Group ◽  
Acid Catalyst ◽  
Protonated Form ◽  
Free Base ◽  
Methyl Substituent ◽  
Methyl Group ◽  
Protective Groups ◽  
Group Migration ◽  
Type 3

Examples of internally alkylated azuliporphyrins were prepared by MacDonald-type “3 + 1” condensations. 2-Methyl- and 2-ethylazulene reacted with an acetoxymethylpyrrole in the presence of an acid catalyst to give azulitripyrranes. Following cleavage of the terminal protective groups, condensation with a diformylpyrrole in the presence of hydrochloric acid and oxidation with ferric chloride afforded 21-alkylazuliporphyrins. An azulene dialdehyde similarly reacted with an [Formula: see text]-methyltripyrrane to generate a 23-methylazuliporphyrin. The products could only be isolated in protonated form and the free-base internally alkylated azuliporphyrins proved to be unstable. Nevertheless, the dications are highly diatropic and the internal alkyl group resonances were shifted upfield to beyond -3 ppm. Reaction of a 23-methylazuliporphyrin with palladium(II) acetate primarily afforded a palladium(II) complex with loss of the internal methyl substituent. However, two palladium(II) benzocarbaporphyrins were also identified that were formed by sequential oxidative ring contraction and methyl group migration. Internally alkylated azuliporphyrins provide new insights into the reactivity of the system and the results show that the introduction of alkyl substituents within porphyrinoid cavities greatly modifies the properties of these structures.

Methyl group migration in the reactions of alkynyltrialkylborates

1988 ◽  
Vol 29 (33) ◽  
pp. 4181-4184 ◽  
Author(s):  
Andrew Pelter ◽  
Robert A. Drake
Keyword(s):  
Methyl Group ◽  
Group Migration
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