Author:
Pandey Bipin,Zope Umesh R.,Ayyangar Nagaraj R.
Publisher
Royal Society of Chemistry (RSC)
Reference29 articles.
1. Baeyer-Villiger oxidation of hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-3,10-dione systems
2. ⊼-Facial Stereoselectivity in Diels-Alder Reaction of Hexacyclo [7.4.2.01,9.03,7.04,14.06,15] Pentadecane-10,12-diene-2,8-dione
3. .pi.-Facial selectivity in Diels-Alder reactions of hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-5,7-diene-3,10-dione
4. For stereospecificity in singlet oxygen addition, B.Pandey, U. R.Zope, P. R.Rajamohanan, and N. R.Ayyangar, submitted for publication.
5. The generality of regioselective Baeyer–Villiger oxidation in many similar systems has been established; B.Pandey and P. V.Dalvi, unpublished work.
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1. A DFT investigation of Diels-Alder reaction of ethyl propiolate to the cage-annulated hexacyclo[7.5.2.01,6.06,13.08,12.010,14]hexadeca-2,4-diene-7,16-dione;Journal of the Serbian Chemical Society;2018
2. π-Facial selectivities and proximal/distal regioselectivities in Diels–Alder reactions of unsymmetrical, cage-annulated 1,3-cyclohexadienes;Tetrahedron;2001-10
3. Reaction of vinylmagnesium bromide with hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-5,7-diene-3,10-dione: Transannular hemiketal formation;Journal of Chemical Crystallography;1996-06
4. Efficient cleavage of cyclopropyl bond by adjacent ketyl radical generated under PET conditions;Tetrahedron;1994-03
5. Studies on cyclobutyl bond cleavage by adjacent ketyl radical generated under PET conditions;Tetrahedron;1994-03