01047nas a2200229 4500008004100000022001400041245007900055210006900134260007500203300001000278520024800288653001400536653001500550653001700565653002100582653001600603100002400619700002000643700002300663700002300686856010800709 2007 eng d a0936-521400aPractical and facile approach towards indole alkaloids: (-)-mitralactonine0 aPractical and facile approach towards indole alkaloids mitralact aRUDIGERSTR 14, D-70469 STUTTGART, GERMANYbGEORG THIEME VERLAG KGcJAN a79-823 a
An efficient approach to (-)-mitralactonine using Pictet-Spengler cyclisation with a highly functionalised masked aldehyde is described. Sharpless asymmetric dihydroxylation (SAD) is utilised to introduce chirality in the key substrate.
10aalkaloids10aasymmetric10acyclisations10adihydroxylations10athioacetats1 aChavan, Subhash, P.1 aSharma, Pallavi1 aSivappa, Rasapalli1 aKalkote, Uttam, R. uhttp://library.ncl.res.in/content/practical-and-facile-approach-towards-indole-alkaloids-mitralactonine