Highly exo selective, photochemically promoted cyclization of iodoallene derivatives
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2022
Authors
Jovanović, Miloš
Simić, Milena

Petković, Miloš

Tasić, Gordana

Maslak, Veselin

Jovanović, Predrag

Savić, Vladimir

Article (Published version)

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A photochemically promoted intramolecular cyclization of aryl-, vinyl-, and alkyliodo allenes has been developed. The optimal conditions employed [Ir(ppy)2(dtbbpy)]PF6 (1 mol%) as catalyst affording products with high exo selectivity in moderate to good yields. Chiral substrates showed diastereoselectivity of up to 95/5 favoring trans product.
Source:
Journal of Heterocyclic Chemistry, 2022, 59, 8, 1435-1440Publisher:
- Wiley Periodicals LLC
Funding / projects:
DOI: 10.1002/jhet.4472
ISSN: 0022-152X
WoS: 000766376800001
Scopus: 2-s2.0-85125948339
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PharmacyTY - JOUR AU - Jovanović, Miloš AU - Simić, Milena AU - Petković, Miloš AU - Tasić, Gordana AU - Maslak, Veselin AU - Jovanović, Predrag AU - Savić, Vladimir PY - 2022 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4175 AB - A photochemically promoted intramolecular cyclization of aryl-, vinyl-, and alkyliodo allenes has been developed. The optimal conditions employed [Ir(ppy)2(dtbbpy)]PF6 (1 mol%) as catalyst affording products with high exo selectivity in moderate to good yields. Chiral substrates showed diastereoselectivity of up to 95/5 favoring trans product. PB - Wiley Periodicals LLC T2 - Journal of Heterocyclic Chemistry T1 - Highly exo selective, photochemically promoted cyclization of iodoallene derivatives VL - 59 IS - 8 SP - 1435 EP - 1440 DO - 10.1002/jhet.4472 ER -
@article{ author = "Jovanović, Miloš and Simić, Milena and Petković, Miloš and Tasić, Gordana and Maslak, Veselin and Jovanović, Predrag and Savić, Vladimir", year = "2022", abstract = "A photochemically promoted intramolecular cyclization of aryl-, vinyl-, and alkyliodo allenes has been developed. The optimal conditions employed [Ir(ppy)2(dtbbpy)]PF6 (1 mol%) as catalyst affording products with high exo selectivity in moderate to good yields. Chiral substrates showed diastereoselectivity of up to 95/5 favoring trans product.", publisher = "Wiley Periodicals LLC", journal = "Journal of Heterocyclic Chemistry", title = "Highly exo selective, photochemically promoted cyclization of iodoallene derivatives", volume = "59", number = "8", pages = "1435-1440", doi = "10.1002/jhet.4472" }
Jovanović, M., Simić, M., Petković, M., Tasić, G., Maslak, V., Jovanović, P.,& Savić, V.. (2022). Highly exo selective, photochemically promoted cyclization of iodoallene derivatives. in Journal of Heterocyclic Chemistry Wiley Periodicals LLC., 59(8), 1435-1440. https://doi.org/10.1002/jhet.4472
Jovanović M, Simić M, Petković M, Tasić G, Maslak V, Jovanović P, Savić V. Highly exo selective, photochemically promoted cyclization of iodoallene derivatives. in Journal of Heterocyclic Chemistry. 2022;59(8):1435-1440. doi:10.1002/jhet.4472 .
Jovanović, Miloš, Simić, Milena, Petković, Miloš, Tasić, Gordana, Maslak, Veselin, Jovanović, Predrag, Savić, Vladimir, "Highly exo selective, photochemically promoted cyclization of iodoallene derivatives" in Journal of Heterocyclic Chemistry, 59, no. 8 (2022):1435-1440, https://doi.org/10.1002/jhet.4472 . .