A formal synthesis of crinipellin B based on the arene-alkene meta-photocycloaddition reaction
摘要:
Starting from triethyl phosphonopropionate and 3-nitro-2-methylbenzoic acid, a formal synthesis of crinipellin B was achieved. The strategy draws on the use of a novel version of the arene-alkene meta-photocycloaddition reaction that proceeds with the generation of 4 rings and 4 quaternary stereocenters in one synthetic operation. (C) 1998 Elsevier Science Ltd. All rights reserved.
A formal synthesis of crinipellin B based on the arene-alkene meta-photocycloaddition reaction
摘要:
Starting from triethyl phosphonopropionate and 3-nitro-2-methylbenzoic acid, a formal synthesis of crinipellin B was achieved. The strategy draws on the use of a novel version of the arene-alkene meta-photocycloaddition reaction that proceeds with the generation of 4 rings and 4 quaternary stereocenters in one synthetic operation. (C) 1998 Elsevier Science Ltd. All rights reserved.
A formal synthesis of crinipellin B based on the arene-alkene meta-photocycloaddition reaction
作者:Paul A. Wender、Timothy M. Dore
DOI:10.1016/s0040-4039(98)01965-0
日期:1998.11
Starting from triethyl phosphonopropionate and 3-nitro-2-methylbenzoic acid, a formal synthesis of crinipellin B was achieved. The strategy draws on the use of a novel version of the arene-alkene meta-photocycloaddition reaction that proceeds with the generation of 4 rings and 4 quaternary stereocenters in one synthetic operation. (C) 1998 Elsevier Science Ltd. All rights reserved.