148441-23-0Relevant academic research and scientific papers
Asymmetric synthesis of pent-3-yl (R)-6-methyl-cyclohex-1-ene carboxylate
Garrido, Narciso M.,Diez, David,Dominguez, Sara H.,Garcia, Mercedes,Sanchez, M. Rosa,Davies, Stephen G.
, p. 2183 - 2186 (2007/10/03)
An expeditious asymmetric synthesis of pent-3-yl (R)-6-methyl-cyclohex-1-enecarboxylate has been achieved in four steps in 42% overall yield employing as the key step a domino reaction initiated by a highly diastereoselective lithium amide 1,4-conjugate a
Herbicidal substituted cycloalkenes
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, (2008/06/13)
Herbicidal substituted cycloalkenes of the formula STR1 in which A is a straight-chain or branched, optionally substituted alkanediyl group, X is O, S, N--R8 or CR9 R10, Y is O, S, NH or N-alkyl, Z is N or R11,
