Literature DB >> 23814320

INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTS.

Tadeusz F Molinski1, Brandon I Morinaka.   

Abstract

Year:  2012        PMID: 23814320      PMCID: PMC3694619          DOI: 10.1016/j.tet.2011.12.070

Source DB:  PubMed          Journal:  Tetrahedron        ISSN: 0040-4020            Impact factor:   2.457


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  196 in total

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2.  Complete structure of the mycolactones.

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3.  Absolute stereochemistry of ulapualide A.

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4.  Synthesis of the DEF-bis-spiroacetal of spirastrellolide A exploiting a double asymmetric dihydroxylation/spiroacetalisation strategy.

Authors:  Ian Paterson; Edward A Anderson; Stephen M Dalby; Jong Ho Lim; Philip Maltas; Christian Moessner
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5.  Structures of new amphidinols with truncated polyhydroxyl chain and their membrane-permeabilizing activities.

Authors:  Nagy Morsy; Toshihiro Houdai; Shigeru Matsuoka; Nobuaki Matsumori; Seiji Adachi; Tohru Oishi; Michio Murata; Takashi Iwashita; Tsuyoshi Fujita
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6.  Combinatorial synthesis of the 1,5-polyol system based on cross metathesis: structure revision of amphidinol 3.

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7.  Bistramides A, B, C, D, and K: a new class of bioactive cyclic polyethers from Lissoclinum bistratum.

Authors:  J F Biard; C Roussakis; J M Kornprobst; D Gouiffes-Barbin; J F Verbist; P Cotelle; M P Foster; C M Ireland; C Debitus
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8.  Spirastrellolide A, an antimitotic macrolide isolated from the Caribbean marine sponge Spirastrella coccinea.

Authors:  David E Williams; Michel Roberge; Rob Van Soest; Raymond J Andersen
Journal:  J Am Chem Soc       Date:  2003-05-07       Impact factor: 15.419

9.  Structure revision and absolute configuration of malhamensilipin A from the freshwater chrysophyte Poterioochromonas malhamensis.

Authors:  Alban R Pereira; Tara Byrum; Grant M Shibuya; Christopher D Vanderwal; William H Gerwick
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Review 10.  Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy.

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  13 in total

1.  Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A.

Authors:  Ikenna E Ndukwe; Xiao Wang; Nelson Y S Lam; Kristaps Ermanis; Kelsey L Alexander; Matthew J Bertin; Gary E Martin; Garrett Muir; Ian Paterson; Robert Britton; Jonathan M Goodman; Eric J N Helfrich; Jörn Piel; William H Gerwick; R Thomas Williamson
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Review 2.  Recent trends in the structural revision of natural products.

Authors:  Bhuwan Khatri Chhetri; Serge Lavoie; Anne Marie Sweeney-Jones; Julia Kubanek
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3.  Unequivocal determination of complex molecular structures using anisotropic NMR measurements.

Authors:  Yizhou Liu; Josep Saurí; Emily Mevers; Mark W Peczuh; Henk Hiemstra; Jon Clardy; Gary E Martin; R Thomas Williamson
Journal:  Science       Date:  2017-04-07       Impact factor: 47.728

4.  Antifungal Diterpene Alkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational Assignments of Agelasidines and Agelasines.

Authors:  E Paige Stout; Lily C Yu; Tadeusz F Molinski
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5.  Halisphingosines A and B, modified sphingoid bases from Haliclona tubifera. Assignment of configuration by circular dichroism and van't Hoff's principle of optical superposition.

Authors:  Tadeusz F Molinski; Renata Biegelmeyer; E Paige Stout; Xiao Wang; Mario L C Frota; Amelia T Henriques
Journal:  J Nat Prod       Date:  2012-12-26       Impact factor: 4.050

Review 6.  Recent advances and applications of experimental technologies in marine natural product research.

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7.  Antioxidative Polyketones from the Mangrove-Derived Fungus Ascomycota sp. SK2YWS-L.

Authors:  Chunbin Tan; Zhaoming Liu; Senhua Chen; Xishan Huang; Hui Cui; Yuhua Long; Yongjun Lu; Zhigang She
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8.  Erylusamides: Novel Atypical Glycolipids from Erylus cf. deficiens.

Authors:  Helena Gaspar; Adele Cutignano; Laura Grauso; Nuno Neng; Vasco Cachatra; Angelo Fontana; Joana Xavier; Marta Cerejo; Helena Vieira; Susana Santos
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Review 9.  The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research.

Authors:  James B McAlpine; Shao-Nong Chen; Andrei Kutateladze; John B MacMillan; Giovanni Appendino; Andersson Barison; Mehdi A Beniddir; Maique W Biavatti; Stefan Bluml; Asmaa Boufridi; Mark S Butler; Robert J Capon; Young H Choi; David Coppage; Phillip Crews; Michael T Crimmins; Marie Csete; Pradeep Dewapriya; Joseph M Egan; Mary J Garson; Grégory Genta-Jouve; William H Gerwick; Harald Gross; Mary Kay Harper; Precilia Hermanto; James M Hook; Luke Hunter; Damien Jeannerat; Nai-Yun Ji; Tyler A Johnson; David G I Kingston; Hiroyuki Koshino; Hsiau-Wei Lee; Guy Lewin; Jie Li; Roger G Linington; Miaomiao Liu; Kerry L McPhail; Tadeusz F Molinski; Bradley S Moore; Joo-Won Nam; Ram P Neupane; Matthias Niemitz; Jean-Marc Nuzillard; Nicholas H Oberlies; Fernanda M M Ocampos; Guohui Pan; Ronald J Quinn; D Sai Reddy; Jean-Hugues Renault; José Rivera-Chávez; Wolfgang Robien; Carla M Saunders; Thomas J Schmidt; Christoph Seger; Ben Shen; Christoph Steinbeck; Hermann Stuppner; Sonja Sturm; Orazio Taglialatela-Scafati; Dean J Tantillo; Robert Verpoorte; Bin-Gui Wang; Craig M Williams; Philip G Williams; Julien Wist; Jian-Min Yue; Chen Zhang; Zhengren Xu; Charlotte Simmler; David C Lankin; Jonathan Bisson; Guido F Pauli
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10.  Total synthesis and complete configurational assignment of amphirionin-2.

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Journal:  Chem Sci       Date:  2020-11-20       Impact factor: 9.825

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