Sources of common compounds: 2343-22-8

Although many compounds look similar to this compound(2343-22-8)Electric Literature of C8H8FN, numerous studies have shown that this compound(SMILES:FC1=CC2=C(NCC2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5-Fluoroindoline( cas:2343-22-8 ) is researched.Electric Literature of C8H8FN.Shi, Yunkai; Chen, Chao; Yang, Yaxi; Bing, zhou published the article 《Rh(III)-catalyzed selective C7-H functionalization of indolines with 1,3-enynes enables access to six-membered 1,7-fused indolines》 about this compound( cas:2343-22-8 ) in Tetrahedron Letters. Keywords: fused indoline preparation diastereoselective; indoline enyne cyclization rhodium catalyst. Let’s learn more about this compound (cas:2343-22-8).

Herein a Rh(III)-catalyzed C7-selective C-H activation/annulation of indolines I (R = H, OMe, F; R1 = H, Me, Br, Cl, F, OMe; R2 = H, Me; R3 = H, Me; R4 = H; R3R4 = -(CH2)5-; R5 = H, Me; R4R5 = -CH=CH-CH=CH-) with 1,3-enynes R6CCCH=C(CH3)2 (R6 = n-Bu, cyclopropyl, Ph, etc.) to efficiently access various privileged 1,7-fused indolines II bearing an all-carbon quaternary stereogenic carbon center was described. Notably, the resulting products II (R = R1 = R2 = R3 = R4 = R5 = H; R6 = cyclopropyl) can be readily transformed into 1,7-fused indoles III, further widening the C-7 derivatization of indoles and highlighting the synthetic utility of this methodol.

Although many compounds look similar to this compound(2343-22-8)Electric Literature of C8H8FN, numerous studies have shown that this compound(SMILES:FC1=CC2=C(NCC2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics