Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine (2015)
- Authors:
- Autor USP: EMERY, FLAVIO DA SILVA - FCFRP
- Unidade: FCFRP
- DOI: 10.1016/j.tetlet.2015.03.039
- Subjects: ALCALOIDES; PALÁDIO; CATALISADORES; PRODUTOS NATURAIS
- Language: Inglês
- Imprenta:
- Publisher place: Kidlington
- Date published: 2015
- Source:
- Título: Tetrahedron Letters
- ISSN: 0040-4039
- Volume/Número/Paginação/Ano: v. 56, n. 18, p. 2307-2310, 2015
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, v. 56, n. 18, p. 2307-2310, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.03.039. Acesso em: 11 fev. 2026. -
APA
Fumagalli, F., & Emery, F. da S. (2015). Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, 56( 18), 2307-2310. doi:10.1016/j.tetlet.2015.03.039 -
NLM
Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039 -
Vancouver
Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2026 fev. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039 - A review of the synthetic strategies for the development of BODIPY dyes for conjugation with proteins
- On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by clik chemistry reactions
- On the synthesis of quinone-based BODIPY hybrids: New insights on antitumor activity and mechanism of action in cancer cells
- Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes
- Naftotiazóis inibidores de dihidroorotato desidrogenase potenciais agentes leishmanicidas
- Síntese de análogos heterocíclicos do aripiprazol
- Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones
- Oral administration of peptide-based drugs: beyond Lipinski's rule
- Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives
- Claisen rearrangement of hydroxynaphthoquinones: selectivity toward naphthofuran or α-xiloidone using copper salts and iodine
Informações sobre o DOI: 10.1016/j.tetlet.2015.03.039 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas