83327-22-4

Usage

InChI:InChI=1/C20H18O8/c1-24-13-7-11(8-14(25-2)17(13)23)18-15(9-21)26-12-5-3-10-4-6-16(22)27-19(10)20(12)28-18/h3-8,15,18,21,23H,9H2,1-2H3/t15-,18-/m1/s1

Upstream product

• 20675-96-1 trans-sinapyl alcohol 
• 486-35-1 daphnetin 
• 477770-79-9 8-acetoxy-7-hydroxycoumarin 
• 477770-81-3 threo-(1R,2R)-1-(4'-benzyloxy-3',5'-dimethoxyphenyl)-3-O-tosyl-1,2-glycol 
• 65535-51-5 8-acetoxy-7-benzyloxycoumarin 
• 65535-49-1 8-acetyl-7-benzyloxycoumarin 
• 65535-50-4 7-Benzyloxy-8-hydroxycoumarin 
• 6748-68-1 8-acetyl-7-hydroxycoumarin 
• 10387-49-2 7-acetyloxycoumarin 
• 93-35-6 7-hydroxy-2H-chromen-2-one 
• 90985-68-5 (E)-4-acetoxy-3,5-dimethoxycinnamic acid 
• 530-59-6 trans-3,5-dimethoxy-4-hydroxycinnamic acid 

Relevant academic research and scientific papers

First enantioselective synthesis of daphneticin and its regioisomer

An enantioselective total synthesis of chiral daphneticin and its regioisomer is reported for the first time.

SYNTHESES OF NATURAL COUMARINOLIGANDS: OXIDATIVE COUPLING OF 7,8-DIHYDROXYCOUMARINS AND PHENYLPROPENES IN THE PRESENCE OF DIPHENYL SELENOXIDE

Oxidative coupling of 7,8-dihydroxycoumarins (1,2) and phenylpropenes (3-5) using Ph2SeO as oxidizing agent resulted in remarkably efficient synthesis of naturally occuring coumarinoligands (cleomiscosin A (6A), aquillochin (cleomiscosin C) (6B), daphneticin (6c), and propacin(6D).

Synthesis and Structural Elucidation of Coumarinolignans

Coumarinolignans are a relatively new class of natural products combining a coumarin skeleton with a phenylpropene moiety.We describe here details of the first biomimetic syntheses of compounds in this series (1-16) utilizing both chemical and enzymatic approaches and the application of the selective INEPT nmr technique for unambiguous structure assignment.Chemical oxidation using silver oxide as an oxidizing agent typically produced two regioisomeric trans-substituted coumarinolignans.Enzymatic oxidation on the other hand normally gave rise to a single regioisomer.Almost all of the known natural coumarinolignans and several new compounds which may subsequently be obtained as natural products were synthesized.Three nmr strategies are described for the structure elucidation of the coumarinolignans, but only one of these techniques, the selective INEPT method, affords an unambiguous structure when only one regioisomer is present.Using this technique the structures and complete proton and carbon-13 chemical shift assignments of sixteen synthetic coumarinolignans were established.The described nmr strategy should prove useful for the unambiguous structure determination of all natural 2-aryl benzodioxanes, including the flavonolignans, the xanthonolignans and certain neolignans.