| Title : Synthesis of stable isotopically labelled 3-methylfuran-2(5H)-one and the corresponding strigolactones - Cheng_2015_J.Labelled.Comp.Radiopharm_58_355 |
| Author(s) : Cheng Y , Ding WH , Long Q , Zhao M , Yang J , Li XQ |
| Ref : J Labelled Comp Radiopharm , 58 :355 , 2015 |
|
Abstract :
Conventional synthetic procedures of strigolactones (SLs) involve the independent synthesis of ring ABC and ring D, followed by a coupling of the two fragments. Here we prepared three kinds of stable, isotopically labelled D-ring analogues productively using a facile protocol. Then, a coupling of the D-rings to ring ABC produced three isotope-labelled SL derivatives. Moreover, (+)-D3-2'-epi-1A and (-)-ent-D3-2'-epi-1A with high enantiomeric purity were obtained via chiral resolution. |
| PubMedSearch : Cheng_2015_J.Labelled.Comp.Radiopharm_58_355 |
| PubMedID: 26179068 |
Cheng Y, Ding WH, Long Q, Zhao M, Yang J, Li XQ (2015)
Synthesis of stable isotopically labelled 3-methylfuran-2(5H)-one and the corresponding strigolactones
J Labelled Comp Radiopharm
58 :355
Cheng Y, Ding WH, Long Q, Zhao M, Yang J, Li XQ (2015)
J Labelled Comp Radiopharm
58 :355