Unknown

Dataset Information

0

Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates.


ABSTRACT: A simple method has been developed for the synthesis of cyclopropa[c]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the acetic acid-induced intramolecular transesterification of 2-arylcyclopropane-1,1-dicarboxylates, was found to be efficient for substrates containing hydroxy group directly attached to the aromatic ring.

SUBMITTER: Ivanova OA 

PROVIDER: S-EPMC6337311 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Convenient Synthesis of Functionalized Cyclopropa[<i>c</i>]coumarin-1a-carboxylates.

Ivanova Olga A OA   Andronov Vladimir A VA   Levina Irina I II   Chagarovskiy Alexey O AO   Voskressensky Leonid G LG   Trushkov Igor V IV  

Molecules (Basel, Switzerland) 20181224 1


A simple method has been developed for the synthesis of cyclopropa[<i>c</i>]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the acetic acid-induced intramolecular transesterification of 2-arylcyclopropane-1,1-dicarboxylates, was found to be efficient for substrates containing hydroxy group directly attached to the aromatic ring. ...[more]

Similar Datasets

| S-EPMC7601631 | biostudies-literature
| S-EPMC9091482 | biostudies-literature
| S-EPMC9037808 | biostudies-literature
| S-EPMC4273213 | biostudies-literature
| S-EPMC8933478 | biostudies-literature
| S-EPMC4015188 | biostudies-literature
| S-EPMC7998207 | biostudies-literature
| S-EPMC9322071 | biostudies-literature
| S-EPMC2533708 | biostudies-literature
| S-EPMC8401603 | biostudies-literature