Synthesis of a cumyl analogue in nitrothiazole series and SRN1 reaction at tertiary carbon
摘要:
A new alkylating agent, 2-(1-methyl-1-nitroethyl)-5-nitrothiazole, bearing a tertiary nitro nucleofuge, reacts with 2-nitropropane anion by S(RN)1 mechanism leading to the C-alkylation product. (C) 1997 Elsevier Science Ltd.