On the stereochemistry of the Pictet-Spengler reaction
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (43) , 5181-5184
- https://doi.org/10.1016/s0040-4039(00)95623-5
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The formation and intramolecular acylation of a 1,2-dihydro-β-carboline derivative; a model sequence for the total synthesis of fumitremorgins.Tetrahedron Letters, 1986
- Total synthesis of fumitremorgin BTetrahedron Letters, 1986
- Synthetic approach to the total synthesis of fumitremorgins II synthesis of optically active pentacyclic intermediates and their dehydrogenationTetrahedron Letters, 1986
- Mechanisms of the thermal isomerization about the C:N+ bond of some iminium saltsThe Journal of Organic Chemistry, 1985
- The Total Synthesis of (—)-DihydrocorynantheolHETEROCYCLES, 1985
- Total Synthesis of (-)-AntirhineHETEROCYCLES, 1985
- General method for the assignment of stereochemistry of 1,3-disubstituted 1,2,3,4-tetrahydro-.beta.-carbolines by carbon-13 spectroscopyJournal of the American Chemical Society, 1980
- The Spiroindolenine Intermediate, a ReviewHETEROCYCLES, 1978
- Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amidesTetrahedron, 1975
- A Correlation of Reaction RatesJournal of the American Chemical Society, 1955