Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Cristina I. Canché Chay"'
Autor:
Cristina I. Canché Chay, Rocío Gómez Cansino, Clara I. Espitia Pinzón, Rubén O. Torres-Ochoa, Roberto Martínez
Publikováno v:
Marine Drugs, Vol 12, Iss 4, Pp 1757-1772 (2014)
Caulerpin (1a), a bis-indole alkaloid from the marine algal Caulerpa sp., was synthesized in three reaction steps with an overall yield of 11%. The caulerpin analogues (1b–1g) were prepared using the same synthetic pathway with overall yields betwe
Externí odkaz:
https://doaj.org/article/766c9b037f3746499fba44330571438f
Autor:
Rocío Gómez Cansino, Roberto Martinez, Cristina I. Canché Chay, Clara Ines Espitia Pinzon, Rubén O. Torres-Ochoa
Publikováno v:
Marine Drugs
Marine Drugs, Vol 12, Iss 4, Pp 1757-1772 (2014)
Marine Drugs; Volume 12; Issue 4; Pages: 1757-1772
Marine Drugs, Vol 12, Iss 4, Pp 1757-1772 (2014)
Marine Drugs; Volume 12; Issue 4; Pages: 1757-1772
Caulerpin (1a), a bis-indole alkaloid from the marine algal Caulerpa sp., was synthesized in three reaction steps with an overall yield of 11%. The caulerpin analogues (1b–1g) were prepared using the same synthetic pathway with overall yields betwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52ea7822c18dd84b797cad574a059178
http://europepmc.org/articles/PMC4012461
http://europepmc.org/articles/PMC4012461