Asymmetric pictet-spengler synthesis of tetrahydroisoquinolines. An enantioselective synthesis of (−)-laudanosine.
- 24 June 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (26) , 2995-2996
- https://doi.org/10.1016/0040-4039(91)80669-w
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Asymmetric synthesis of 2-alkyl(aryl)-2,3-dihydro-4-pyridones by addition of Grignard reagents to chiral 1-acyl-4-methoxypyridinium saltsThe Journal of Organic Chemistry, 1990
- Enantioselective synthesis of isoquinoline alkaloidsCanadian Journal of Chemistry, 1986
- Synthesis of E- and Z-vinyl ethers by the Horner–Wittig reactionJournal of the Chemical Society, Perkin Transactions 1, 1979
- A biogenetic type synthesis of S(+)-laudanosine from L(-)-dopaTetrahedron Letters, 1972
- New Synthesis of 1-Benzyl-6, 7-dihydroxy-1, 2, 3, 4-tetrahydroisoquinoline DerivativesCHEMICAL & PHARMACEUTICAL BULLETIN, 1970
- A novel synthesis of 1,2,3,4-tetrahydroisoquinolines and a note on the reactivity of a 4-methoxy-derivativeJournal of the Chemical Society D: Chemical Communications, 1969