Electrooxidative cleavage of carbon-carbon linkages. 1. Preparation of acyclic oxoalkanoates from 2-hydroxy- and 2-acetoxy-1-cycloalkanones and cycloalkanone enol acetates
Electrooxidative cleavage of carbon-carbon linkages. 1. Preparation of acyclic oxoalkanoates from 2-hydroxy- and 2-acetoxy-1-cycloalkanones and cycloalkanone enol acetates
α-Nitro Ketones; 8<sup>1</sup>. Nitration of Enol Acetates with Trifluoroacetic Anhydride and Ammonium Nitrate
作者:Pimchit Dampawan、Walter W. Zajac, Jr.
DOI:10.1055/s-1983-30417
日期:——
.alpha.-Nitro ketones. 6. Synthesis and conformation of 2-methyl-2-nitro-, cis- and trans-6-methyl-2-nitro-, and cis- and trans-2,6-dimethyl-2-nitrocyclohexanones
作者:Pimchit Dampawan、Walter W. Zajac
DOI:10.1021/jo00346a006
日期:1982.3
TORII, SIGERU;INOKUCHI, TSUTOMU;OI, RYU, J. ORG. CHEM., 1982, 47, N 1, 47-52
作者:TORII, SIGERU、INOKUCHI, TSUTOMU、OI, RYU
DOI:——
日期:——
DAMPAWAN, P.;ZAJAC, W. W. ,JR., SYNTHESIS, BRD, 1983, N 7, 545-546
作者:DAMPAWAN, P.、ZAJAC, W. W. ,JR.
DOI:——
日期:——
Electrooxidative cleavage of carbon-carbon linkages. 1. Preparation of acyclic oxoalkanoates from 2-hydroxy- and 2-acetoxy-1-cycloalkanones and cycloalkanone enol acetates