The stereospecific synthesis of trans-1,3-disubstituted-1,2,3,4\_tetrahydro $-carbolines has been accomplished in good yield by a two step sequence which involves Pi&et-Spengler condensation of Nb-benzyltryptophan methyl: ester with aldehydes, followed by removal of the 2-benzyl moiety from the corr
✦ LIBER ✦
Crystal and molecular structure of aN(2)-benzyl-1,3-disubstituted-1,2,3,4-tetrahydro-β-carboline
✍ Scribed by Judith H. Everett; Colin D. Reynolds; Catherine A. Sparks; Walter Pangborn; Patrick D. Bailey; Zbigniew Dauter; Madeleine Helliwell; Sean P. Hollinshead
- Publisher
- Springer
- Year
- 1990
- Tongue
- English
- Weight
- 373 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1572-8854
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