A simple access to hexahydropyrimidine from 1,3-diamine: synthesis and solid-state characterization
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02234-9.pdf
Reference47 articles.
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2. Guggisberg A, Drandarov K, Hesse M (2000) Protoverbine, the parent member of a class of macrocyclic spermine alkaloids. HCA 83:3035–3042. https://doi.org/10.1002/1522-2675(20001108)83:11%3c3035::AID-HLCA3035%3e3.0.CO;2-P
3. Drandarov K, Guggisberg A, Hesse M (1999) Macrocyclic spermine alkaloids from Verbascum: the (E/Z)-isomeric pairs (−)-(S)-verbasitrine/(−)-(S)-isoverbasitrine and (+)-(S)-verbametrine/(+)-(S)-isoverbametrine: isolation, structure elucidation, and synthesis. HCA 82:229–237. https://doi.org/10.1002/(SICI)1522-2675(19990210)82:2%3c229::AID-HLCA229%3e3.0.CO;2-H
4. Perillo IA, García MB, Bisceglia JÁ, Orelli LR (2022) N-Arylhexahydropyrimidines. Part 1. Synthesis and 1 H NMR characterization of 1,3-Di and 1,2,3-trisubstituted derivatives. J Heterocycl Chem 39:655–661. https://doi.org/10.1002/jhet.5570390409
5. Verma S, Kumar S, Jain SL, Sain B (2011) Thiourea dioxide promoted efficient organocatalytic one-pot synthesis of a library of novel heterocyclic compounds. Org Biomol Chem 9:6943. https://doi.org/10.1039/c1ob05818e
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