Results 251 to 260 of about 108,684 (302)
Some of the next articles are maybe not open access.

Büchner ring expansion

2009
Reaction of a phenyl ring with a diazoacetic ester to give a cyclohepta–2,4,6– trienecarboxylic acid ester. Intramolecular Buchner reaction is more useful in synthesis. Cf. Pfau–Platter azulene synthesis.
openaire   +1 more source

Ring expansions and contractions of metalloporphyrins

Dalton Transactions, 2008
Ring expansions or contractions of metalloporphyrins are unusual reactions. In this review, the author will show how the step by step analysis of two serendipitous reactions allows one to unveil their mechanism and to point out the key role of nickel ion in these rearrangements.
openaire   +2 more sources

Synthesis and Ring Expansions of Functionalized Spirocyclobutanones

Organic Letters, 2007
The first condensations between bis(trimethylsilyloxy)cyclobutene derivatives and functionalized orthoesters are reported. The resulting adducts are readily converted into spirocycloethers, which undergo a variety of -CH2- and -O- insertions with excellent regioselectivity.
Nuno, Maulide, István E, Markó
openaire   +2 more sources

A ring expansion reaction of 1,3-oxathiolanes

Chemical Communications, 2002
1,3-Oxathiolanes are efficiently converted, via sulfur ylide intermediates, to 1,4-oxathianes by ring expansion with a silylated diazoacetate in the presence of a copper catalyst.
Maria, Ioannou   +2 more
openaire   +2 more sources

Ring expansions. II. Diazoethane ring expansion of norcamphor

The Journal of Organic Chemistry, 1973
Michael A. McKinney, Parmanand P. Patel
openaire   +1 more source

Ring Expansion

2008
M. Inoue, S. Yamashita
openaire   +2 more sources

Ring-Expansion of Ketones with [1.1.1]Propellane

Journal of the American Chemical Society
Here, we present an approach for the ring-expansion of ketones, enabled by the rare electrophilic activation of [1.1.1]propellane. A broad spectrum of ketones was examined, showcasing excellent compatibility with various functional groups such as ester, amide, and amines. The novel reaction is practical and scalable (up to 56 g).
Ganesh Arjun Kadam   +5 more
openaire   +2 more sources

Ring Expansion

2007
S. V. Ley, L.-G. Milroy, R. M. Myers
openaire   +1 more source

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