4254-15-3, An article , which mentions 4254-15-3, molecular formula is C3H8O2. The compound – (S)-Propane-1,2-diol played an important role in people’s production and life.
Pigments of fungi. Part 41. Synthesis of (S)-(+)- and (+/-)-dermolactone; stereochemistry of dermocactone from the Australian fungus Dermocybe sanguinea (Wulf. ex Fr.) Wuensche sensu Cleland
(S)-(+)-Dermolactone 3 has been synthesised in monochiral form beginning with ethyl (S)-lactate, the tetracyclic nucleus being assembled by way of a regiospecific cycloaddition between the known chloronaphthoquinone 15 and the novel, highly functionalised chiral butadiene 5.Isochiral dermolactone 3 + 4 is prepared in the same way from (+/-)-5.Dermolactone, as it occurs naturally, is shown by 1H NMR shift experimants on the corresponding permethyl ethers 25 and 27, using
4254-15-3, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 4254-15-3
Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate