Pd-catalyzed decarboxylative coupling of arylalkynyl carboxylic acids with allyl ethers: regioselective synthesis of branched 1,3-enynes
-
Add time:07/12/2019 Source:sciencedirect.com
This work reported an efficient and novel method to prepare branched 1,3-enynes via Pd(II)-catalyzed decarboxylative coupling of arylalkynyl carboxylic acids with allylic ethers under mild conditions. Various arylalkynyl carboxylic acids and allylic ethers could participate in the reaction, regioselectively affording the desired branched 1,3-enynes in moderate to good yields.
We also recommend Trading Suppliers and Manufacturers of 4-(4-METHOXY-PHENOXYMETHYL)-BENZOIC ACID (cas 303774-32-5). Pls Click Website Link as below: cas 303774-32-5 suppliers
Prev:Synthesis, characterization and crystal structures of the boratranes: 2,10,11-trioxa-6-aza-1-boratricyclo[4.4.4.01,6] tetradecane (tri-n-propanolamine borate), and 3-(4-methoxy)phenoxymethyl-7,10-dimethyl-2,8,9-trioxa-5-aza-1-boratricyclo[3.3.3.01,5]-undecane
Next:Adsorption and corrosion inhibition characteristics of some organic molecules containing methoxy phenyl moiety on mild steel in hydrochloric acid solution) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis, structure–activity relationship of iodinated-4-aryloxymethyl-coumarins as potential anti-cancer and anti-mycobacterial agents07/14/2019
- Adsorption and corrosion inhibition characteristics of some organic molecules containing methoxy phenyl moiety on mild steel in hydrochloric acid solution07/13/2019
- Synthesis, characterization and crystal structures of the boratranes: 2,10,11-trioxa-6-aza-1-boratricyclo[4.4.4.01,6] tetradecane (tri-n-propanolamine borate), and 3-(4-methoxy)phenoxymethyl-7,10-dimethyl-2,8,9-trioxa-5-aza-1-boratricyclo[3.3.3.01,5]-undecane07/11/2019
-
Health and Chemical more >


