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New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles

Remir Grigorevich Kostyanovsky ¹

Remir Grigorevich Kostyanovsky

Gulnara Konstantinovna Kadorkina ¹

Gulnara Konstantinovna Kadorkina

Anait Genrikovna Mkhitaryan ¹

Anait Genrikovna Mkhitaryan

Ivan Ivanovich Chervin ¹

Ivan Ivanovich Chervin

Abil E Aliev ¹

Abil E Aliev

¹ N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

10.1070/MC1993v003n01ABEH000204

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Published 1993-02-28

Communication , Volume 3, Issue 1, 21-23

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Kostyanovsky R. G. et al. New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles // Mendeleev Communications. 1993. Vol. 3. No. 1. pp. 21-23.

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Kostyanovsky R. G., Kadorkina G. K., Mkhitaryan A. G., Chervin I. I., Aliev A. E. New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles // Mendeleev Communications. 1993. Vol. 3. No. 1. pp. 21-23.

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TY - JOUR

DO - 10.1070/MC1993v003n01ABEH000204

UR - https://mendcomm.colab.ws/publications/10.1070/MC1993v003n01ABEH000204

TI - New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles

T2 - Mendeleev Communications

AU - Kostyanovsky, Remir Grigorevich

AU - Kadorkina, Gulnara Konstantinovna

AU - Mkhitaryan, Anait Genrikovna

AU - Chervin, Ivan Ivanovich

AU - Aliev, Abil E

PY - 1993

DA - 1993/02/28

PB - Mendeleev Communications

SP - 21-23

IS - 1

VL - 3

ER -

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@article{1993_Kostyanovsky,

author = {Remir Grigorevich Kostyanovsky and Gulnara Konstantinovna Kadorkina and Anait Genrikovna Mkhitaryan and Ivan Ivanovich Chervin and Abil E Aliev},

title = {New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles},

journal = {Mendeleev Communications},

year = {1993},

volume = {3},

publisher = {Mendeleev Communications},

month = {Feb},

url = {https://mendcomm.colab.ws/publications/10.1070/MC1993v003n01ABEH000204},

number = {1},

pages = {21--23},

doi = {10.1070/MC1993v003n01ABEH000204}

}

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Kostyanovsky, Remir Grigorevich, et al. “New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles.” Mendeleev Communications, vol. 3, no. 1, Feb. 1993, pp. 21-23. https://mendcomm.colab.ws/publications/10.1070/MC1993v003n01ABEH000204.

Abstract

Newly-found steric limits for the Knorr–Paal reaction in the case of 2-methyl-1,2-propanediamine and acetonylacetone make it possible for the process to occur with only one amino group, giving aminopyrrole 2, and with aziridines, due to dimerization under the conditions of the reaction, giving 1-((β-aziridinoalkyl)pyrroles 4a,b.