53447-44-2
53447-44-2
Chemical Structure
(+)-Monomorine I
- CAS No.: 53447-44-2
- Formula:C13H25N
- Molecular Weight:195.34
SMILES: CCCC[C@H]1N2[C@](CCC[C@@H]2C)([H])CC1
Biological Activity: (+)-Monomorine I is an Indolizidine alkaloid and the enantiomer of Monomorine I. Monomorine I is the trail pheromone of the pharaoh ant Monomorium oharoanasl[1][2][3][4][5][6].
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(+)-Monomorine I | (+)-Monomorine I is an Indolizidine alkaloid and the enantiomer of Monomorine I. Monomorine I is the trail pheromone of the pharaoh ant Monomorium oharoanasl. | |||||||||||||||||||||
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References
- [1]. Xu FF, et al. Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids. Nature communications. 2023 Oct 06;14(1):6251.
- [2]. Saha D, Bagchi S, Sharma A. Metal-catalyzed synthesis of cyclic imines: a versatile scaffold in organic synthesis[J]. Chemistry of Heterocyclic Compounds, 2018, 54(3): 302-313.
- [3]. Soria M J G. Selective synthesis and reactivity of indolizines[D]. Universitat d'Alacant/Universidad de Alicante, 2018.
- [4]. Cole KA. The silver ion-induced rearrangement of N-chloro-octahydropyrindines: A synthesis of monomorine I. The University of Tennessee; 1990.
- [5]. McManus JB, et al. Generation and Alkylation of α-Carbamyl Radicals via Organic Photoredox Catalysis. Journal of the American Chemical Society. 2018 Jul 25;140(29):9056-9060.
- [6]. Michael JP, et al. Simple Indolizidine and Quinolizidine Alkaloids. The Alkaloids. Chemistry and biology. 2016;75:1-498.
