ChemInform Abstract: Seven-Membered Ring Synthesis via Iron-Mediated Carbonylative Ring Expansion and σ-Alkyl-π-allyl Complexes

ChemInform ◽  
2010 ◽  
Vol 27 (36) ◽  
pp. no-no
Author(s):  
P. EILBRACHT ◽  
A. HIRSCHFELDER
ChemInform ◽  
2010 ◽  
Vol 26 (29) ◽  
pp. no-no
Author(s):  
A. HAKIKI ◽  
M. MOSSADAK ◽  
M. MOKHLES ◽  
F. ROUESSAC ◽  
H. DUDDECK ◽  
...  

1974 ◽  
Vol 5 (30) ◽  
pp. no-no
Author(s):  
P. M. COLLINS ◽  
N. N. OPARAECHE ◽  
B. R. WHITTON
Keyword(s):  

2019 ◽  
Vol 10 (43) ◽  
pp. 10129-10134 ◽  
Author(s):  
Sripati Jana ◽  
Zhen Yang ◽  
Chao Pei ◽  
Xinfang Xu ◽  
Rene M. Koenigs

We have shown light mediated ring-expansion reactions of 4-membered ring heterocycles. The reaction proceeds via a diradical mechanism and bond length play a key role in the stereodetermining step.


1999 ◽  
Vol 121 (36) ◽  
pp. 8251-8259 ◽  
Author(s):  
S. Sherry Zhu ◽  
Dustin R. Cefalo ◽  
Daniel S. La ◽  
Jennifer Y. Jamieson ◽  
William M. Davis ◽  
...  
Keyword(s):  

2012 ◽  
Vol 26 (3) ◽  
pp. 232-239 ◽  
Author(s):  
Lili Zhang ◽  
Huiling Liu ◽  
Yuhong Yang ◽  
Zhihui Chong ◽  
Tingting Feng ◽  
...  

2005 ◽  
Vol 44 (29) ◽  
pp. 4608-4611 ◽  
Author(s):  
Takanori Matsuda ◽  
Masaomi Makino ◽  
Masahiro Murakami
Keyword(s):  

2014 ◽  
Vol 67 (9) ◽  
pp. 1288 ◽  
Author(s):  
R. Alan Aitken ◽  
Clémence Hauduc ◽  
M. Selim Hossain ◽  
Emily McHale ◽  
Adrian L. Schwan ◽  
...  

Flash vacuum pyrolysis (FVP) of benzo[c]thiopyran S,S-dioxide (1) results in formation of indene and 2-vinylbenzaldehyde as previously described. A range of eight analogues with various substitution patterns are found to behave differently. In general, there is no extrusion of SO2 to give products analogous to indene, but unsaturated carbonyl products analogous to 2-vinylbenzaldehyde are formed in most cases by way of ring expansion to a 7-membered ring sultine, extrusion of SO, and intramolecular hydrogen atom transfer. Other processes observed include formation of anthracene via an isomeric 7-membered sultine with loss of SO, CO and methane or butane, and formation of 4-ethylidene-4,5-dihydrocyclobuta[b]thiophenes by way of SO loss, a radical rearrangement, and extrusion of acetone. The analogues with a halogen substituent at position 8 on the benzene ring require a higher temperature to react and give naphthalene resulting from net elimination of HX and SO2. The X-ray crystal structure of 1 is also reported.


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