Strategies towards the synthesis of staurosporine indolocarbazole alkaloid and its analogues (2016)
- Authors:
- Autor USP: OLIVEIRA JUNIOR, OSVALDO NOVAIS DE - IFSC
- Unidade: IFSC
- DOI: 10.5772/63832
- Subjects: ALCALOIDES; NEOPLASIAS; PLANEJAMENTO DE FÁRMACOS
- Keywords: Indolocarbazole; Alkaloids; Cancer; Synthesis; Sugar moiety; Glycosylation
- Language: Inglês
- Imprenta:
- Source:
- Título: Scope of selective heterocycles from organic and pharmaceutical perspective
- Volume/Número/Paginação/Ano: 166 p.
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
RAO, B. Purna Chandra e OLIVEIRA JUNIOR, Osvaldo Novais de e VARALA, Ravi. Strategies towards the synthesis of staurosporine indolocarbazole alkaloid and its analogues. Scope of selective heterocycles from organic and pharmaceutical perspective. Tradução . Rijeka: Intech, 2016. p. 166 . Disponível em: https://doi.org/10.5772/63832. Acesso em: 09 nov. 2024. -
APA
Rao, B. P. C., Oliveira Junior, O. N. de, & Varala, R. (2016). Strategies towards the synthesis of staurosporine indolocarbazole alkaloid and its analogues. In Scope of selective heterocycles from organic and pharmaceutical perspective (p. 166 ). Rijeka: Intech. doi:10.5772/63832 -
NLM
Rao BPC, Oliveira Junior ON de, Varala R. Strategies towards the synthesis of staurosporine indolocarbazole alkaloid and its analogues [Internet]. In: Scope of selective heterocycles from organic and pharmaceutical perspective. Rijeka: Intech; 2016. p. 166 .[citado 2024 nov. 09 ] Available from: https://doi.org/10.5772/63832 -
Vancouver
Rao BPC, Oliveira Junior ON de, Varala R. Strategies towards the synthesis of staurosporine indolocarbazole alkaloid and its analogues [Internet]. In: Scope of selective heterocycles from organic and pharmaceutical perspective. Rijeka: Intech; 2016. p. 166 .[citado 2024 nov. 09 ] Available from: https://doi.org/10.5772/63832 - Grid to plate current-voltage characteristics of a corona triode
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Informações sobre o DOI: 10.5772/63832 (Fonte: oaDOI API)
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