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Intramolecular cycloaddition in cyclohexa-2,4-dienone and photochemical reactions: Synthesis of 12-methyl-3-oxa-endo-tricyclo[6.2.2.0(1,6)]dodec-11-en-10-one, and pyran annulated bicyclo[3.3.0]octane and bicyclo[4.2.0]octane frameworks

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Title Intramolecular cycloaddition in cyclohexa-2,4-dienone and photochemical reactions: Synthesis of 12-methyl-3-oxa-endo-tricyclo[6.2.2.0(1,6)]dodec-11-en-10-one, and pyran annulated bicyclo[3.3.0]octane and bicyclo[4.2.0]octane frameworks
 
Creator SINGH, V
SAHU, BC
 
Subject closing metathesis
rearrangement
triquinanes
cycloaddition
intramolecular
photoreaction
cyclohexa-2,4-dienone
oxa-di-pi-methane rearrangement
 
Description Synthesis of pyran annulated bicyclo[2.2.2]octane having a beta,gamma-enone chromophore and its photochemical reaction leading to diquinane-pyran hybrid and pyran annulated bicyclo[4.2.0]octane systems has been described.
 
Publisher COUNCIL SCIENTIFIC & INDUSTRIAL RES
 
Date 2011-07-20T11:16:42Z
2011-12-26T12:51:27Z
2011-12-27T05:36:36Z
2011-07-20T11:16:42Z
2011-12-26T12:51:27Z
2011-12-27T05:36:36Z
2009
 
Type Article
 
Identifier INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 48(8), 1148-1155
0376-4699
http://dspace.library.iitb.ac.in/xmlui/handle/10054/5454
http://hdl.handle.net/10054/5454
 
Language en