Mechanism driven trans stereospecificity in the Pictet-Spengler reaction. Stereospecific formation of trans-1,2,3-trisubstituted-tetrahydro β- carbolines by condensation of Nb-diphenylmethyl tryptophan isopropyl esters wtm aldehydes
- DOI
- 10.1016/s0040-4039(00)61268-6
- Published
- 1992-08
- Container
- Tetrahedron Letters
- Publisher
- Elsevier BV
- Open access
- unknown
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BibTeX
@article{allodium:10.1016/s0040-4039-00-61268-6,
title = {Mechanism driven trans stereospecificity in the Pictet-Spengler reaction. Stereospecific formation of trans-1,2,3-trisubstituted-tetrahydro β- carbolines by condensation of Nb-diphenylmethyl tryptophan isopropyl esters wtm aldehydes},
author = {Kevin M. Czerwinski and Li Deng and James M. Cook},
year = {1992},
journal = {Tetrahedron Letters},
doi = {10.1016/s0040-4039(00)61268-6},
url = {https://doi.org/10.1016/s0040-4039(00)61268-6}
}RIS
TY - JOUR TI - Mechanism driven trans stereospecificity in the Pictet-Spengler reaction. Stereospecific formation of trans-1,2,3-trisubstituted-tetrahydro β- carbolines by condensation of Nb-diphenylmethyl tryptophan isopropyl esters wtm aldehydes AU - Kevin M. Czerwinski AU - Li Deng AU - James M. Cook PY - 1992 JO - Tetrahedron Letters DO - 10.1016/s0040-4039(00)61268-6 UR - https://doi.org/10.1016/s0040-4039(00)61268-6 ER -
APA
Czerwinski, K. M., Deng, L., & Cook, J. M. (1992). Mechanism driven trans stereospecificity in the Pictet-Spengler reaction. Stereospecific formation of trans-1,2,3-trisubstituted-tetrahydro β- carbolines by condensation of Nb-diphenylmethyl tryptophan isopropyl esters wtm aldehydes. Tetrahedron Letters. https://doi.org/10.1016/s0040-4039(00)61268-6
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- crossref · retrieved 2026-09-26T05:01:53.282Z