ChemInform Abstract: Synthetic Studies Toward Complex Polyether Macrolides of Marine Origin

S. D. BURKE; J. R. PHILIPS; K. J. QUINN; G. ZHANG; K. W. JUNG; J. L. BUCHANAN; R. E. PERRI

doi:10.1002/chin.199729285

ChemInform Abstract: Synthetic Studies Toward Complex Polyether Macrolides of Marine Origin

ChemInform ◽

10.1002/chin.199729285 ◽

2010 ◽

Vol 28 (29) ◽

pp. no-no

Author(s):

S. D. BURKE ◽

J. R. PHILIPS ◽

K. J. QUINN ◽

G. ZHANG ◽

K. W. JUNG ◽

...

Keyword(s):

Marine Origin ◽

Synthetic Studies ◽

Polyether Macrolides

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ChemInform Abstract: Synthetic Studies Towards the 2-Aminopyrimidine Alkaloids Variolins and Meridianins from Marine Origin.

ChemInform ◽

10.1002/chin.200036229 ◽

2010 ◽

Vol 31 (36) ◽

pp. no-no

Author(s):

Pilar M. Fresneda ◽

Pedro Molina ◽

Santiago Delgado ◽

Juan A. Bleda

Keyword(s):

Marine Origin ◽

Synthetic Studies

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Synthetic studies towards novel tris-oxazole based macrolides of marine origin. Stereocontrolled synthesis of the C20C35 fragment in ulapualide A

Tetrahedron Letters ◽

10.1016/0040-4039(95)00955-c ◽

1995 ◽

Vol 36 (29) ◽

pp. 5271-5274

Author(s):

Shital K Chattopadhyay ◽

Gerald Pattenden

Keyword(s):

Marine Origin ◽

Stereocontrolled Synthesis ◽

Synthetic Studies

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Synthetic Studies on Aplyronine A, a Potent Antitumor Substance of Marine Origin: Stereocontrolled Synthesis of the C21–C34 Segment

Tetrahedron Letters ◽

10.1016/0040-4039(94)88035-2 ◽

1994 ◽

Vol 35 (8) ◽

pp. 1247-1250 ◽

Cited By ~ 28

Author(s):

Hideo Kigoshi ◽

Makoto Ojika ◽

Kiyotake Suenaga ◽

Tsuyoshi Mutou ◽

Junko Hirano ◽

...

Keyword(s):

Marine Origin ◽

Stereocontrolled Synthesis ◽

Synthetic Studies ◽

Aplyronine A

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Total synthesis of cytotoxic marine macrolides: Callipeltoside A, aurisides A and B, and dolastatin 19

Pure and Applied Chemistry ◽

10.1351/pac200880081773 ◽

2008 ◽

Vol 80 (8) ◽

pp. 1773-1782 ◽

Cited By ~ 12

Author(s):

Ian Paterson ◽

Alison D. Findlay

Keyword(s):

Total Synthesis ◽

Conformational Analysis ◽

Marine Origin ◽

Total Syntheses ◽

Stereochemical Assignment ◽

Callipeltoside A ◽

Marine Macrolides ◽

Synthetic Studies

Synthetic studies pertaining to a novel class of structurally related glycosidic 14-membered macrolides of marine origin are reported. The evolution of a versatile aldol-based strategy that culminated in the total syntheses of callipeltoside A and aurisides A and B is detailed. Using a combination of biogenetic considerations and conformational analysis, a revised stereochemical assignment for the related polyketide dolastatin 19 was proposed and validated by total synthesis.

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Synthetic Studies towards Novel tris-Oxazole based Macrolides of Marine Origin. Stereocontrolled Synthesis of the C20-C35 Fragment in Ulapualide A

Tetrahedron Letters ◽

10.1016/00404-0399(50)0955c- ◽

1995 ◽

Vol 36 (29) ◽

pp. 5271-5274

Author(s):

S Chattopadhyay

Keyword(s):

Marine Origin ◽

Stereocontrolled Synthesis ◽

Synthetic Studies

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Synthetic studies towards the 2-aminopyrimidine alkaloids variolins and meridianins from marine origin

Tetrahedron Letters ◽

10.1016/s0040-4039(00)00728-0 ◽

2000 ◽

Vol 41 (24) ◽

pp. 4777-4780 ◽

Cited By ~ 48

Author(s):

Pilar M Fresneda ◽

Pedro Molina ◽

Santiago Delgado ◽

Juan A Bleda

Keyword(s):

Marine Origin ◽

Synthetic Studies

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ChemInform Abstract: Synthetic Studies Towards Novel tris-Oxazole Based Macrolides of Marine Origin. Stereocontrolled Synhesis of the C20-C35 Fragment (I) in Ulapualide A.

ChemInform ◽

10.1002/chin.199543272 ◽

2010 ◽

Vol 26 (43) ◽

pp. no-no

Author(s):

S. K. CHATTOPADHYAY ◽

G. PATTENDEN

Keyword(s):

Marine Origin ◽

Synthetic Studies

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Synthetic studies toward inducamide C

Organic & Biomolecular Chemistry ◽

10.1039/d0ob01995j ◽

2021 ◽

Author(s):

Ardalan A. Nabi ◽

Lydia M. Scott ◽

Daniel P. Furkert ◽

Jonathan Sperry

Keyword(s):

Natural Product ◽

Structural Revision ◽

Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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