Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 148 checked references that resolve
resolves10.1016/j.ejmech.2012.06.060Laurene-type sesquiterpenes from the Red Sea red alga Laurencia obtusa as potential antitumor–antimicrobial agents
resolves10.1021/jo00129a020Conformational Control in the Cyclization of an Unsaturated Vinyllithium: Synthesis of (.+-.)-Laurene
resolves10.1016/0040-4020(95)00955-8Synthetic applications of the baylis-hillman reaction: Simple synthesis of [2E]-2-butyloct-2-enal and [2E]-2-tridecylheptadec-2-enal
resolves10.1016/S0040-4039(00)87822-3Isolation of 12-(S)-hepe from the red marine alga murrayella periclados and revision of structure of an acyclic icosanoid from laurencia hybrida. Implications to the biosynthesis of the marine prostanoid hybridalactone
resolves10.1071/CH04047Concerning the Proposed Structure of (+)-Laurobtusol: Spectral Discrepancies with Synthetic, Racemic Stereoisomers
resolves10.1039/b302337kThe role of vanadium bromoperoxidase in the biosynthesis of halogenated marine natural products
resolves10.1021/np50071a023Two New Rearranged Sesquiterpenoids from the Red Alga Laurencia obtusa
resolves10.1016/S0040-4020(01)96059-4The structure of laurobtusol, a new rearranged sesquiterpenoid from the mediterranean red alga laurencia obtusa
resolves10.1071/CH9891591Tropical Marine Algae. III. New Sesquiterpenes From
<i>Laurencia majuscula</i>
(Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)
resolves10.1055/s-0030-1250526Antileishmanial Sesquiterpenes from the Brazilian Red Alga<i>Laurencia dendroidea</i>
resolves10.1021/np0102307New Sesquiterpene Derivatives from the Red Alga <i>Laurencia </i><i>s</i><i>coparia.</i> Isolation, Structure Determination, and Anthelmintic Activity
resolves10.1021/jo00121a051Synthesis of Laurencione, a Labile Dihydro-3(2H)-furanone Derivative from the Red Alga Laurencia spectabilis
resolves10.1055/s-1996-4335New Formal Syntheses of Laurencione, a Labile Dihydrofuranone Derivative from the Red Alga Laurencia spectabilis
resolves10.1071/CH9921611Tropical Marine Algae. VIII. The Structural Determination of Novel Sesquiterpenoid Metabolites From the Red Alga
<i>.Laurencia majuscula</i>
resolves10.1016/j.tetlet.2004.07.125Chamigrenelactone, a polyoxygenated sesquiterpene with a novel structural type and devoid of halogen from Laurencia obtusa
resolves10.1021/jo00412a056Poitediol, a new nonisoprenoid sesquiterpene diol from the marine alga Laurencia poitei
resolves10.1071/CH9730345The total synthesis of (±)-laurinterol and related compounds
resolves10.1246/cl.1984.1349LAURENONES A AND B, NEW SESQUITERPENES, FROM THE RED ALGA <i>LAURENCIA NIPPONICA</i> YAMADA
resolves10.1246/cl.1990.1287Biosynthetic Formation of Cyclic Bromo-ethers Initiated by Lactoperoxidase
resolves10.1016/0040-4039(92)88128-REnzymatic Single-step Formation of Laureatin and Its Key Intermediate, Prelaureatin, from (3Z, 6S, 7S)-Laurediol
resolves10.1016/0031-9422(93)85154-JBiogenetic intermediates, (3e and 3z,12z)-laurediols and (3e and 3z)-12,13- dihydrolaurediols, isolated from Laurencia nipponica
resolves10.1515/botm.1992.35.3.227<i>Laurencia viridis </i>sp. nov. (Ceramiales, Rhodomelaceae) from the Macaronesian Archipelagos
resolves10.1002/chem.200305023Calenzanane Sesquiterpenes from the Red Seaweed <i>Laurencia microcladia</i> from the Bay of Calenzana, Elba Island: Acid‐Catalyzed Stereospecific Conversion of Calenzanol into Indene‐ and Guaiazulene‐Type Sesquiterpenes
resolves10.1021/ja204027aCatalysis-Based and Protecting-Group-Free Total Syntheses of the Marine Oxylipins Hybridalactone and the Ecklonialactones A, B, and C
resolves10.1016/0040-4020(81)85020-XHybridalactone, An unusual fatty acid metabolite from the red alga Laurencia hybrida (Rhodophyta, Rhodomelaceae)
resolves10.1039/b101889mThe syntheses of three highly unsaturated marine lipid hydrocarbons
resolves10.1021/jo00337a053Secondary metabolites from a red alga (Laurencia intricata): sesquiterpene alcohols
resolves10.1016/0031-9422(79)80143-0Guadalupol and epiguadalupol, rearranged sesquiterpene alcohols from Laurencia snyderiae var. guadalupensis
resolves10.1021/ja00461a045Neoconcinndiol hydroperoxide, a novel marine diterpenoid from the red alga Laurencia
resolves10.1016/0040-4039(94)02329-AEnzymatic reaction of (3E,6S,7S)-laurediol and the molecular modeling studies on the cyclization of laurediols
resolves10.1002/hlca.200790044Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga <i>Laurencia similis</i> (Rhodomelaceae)
resolves10.1021/np070378bDiterpenes, Sesquiterpenes, and a C<sub>15</sub>-Acetogenin from the Marine Red Alga <i>Laurencia mariannensis</i>
resolves10.1021/np0701172Laurendecumallenes A–B and Laurendecumenynes A–B, Halogenated Nonterpenoid C<sub>15</sub>-Acetogenins from the Marine Red Alga Laurencia decumbens
resolves10.1080/14786410802019309Laurane-derived sesquiterpenes from the marine red alga<b><i>Laurencia tristicha</i></b>(Rhodomelaceae)
resolves10.1016/j.bse.2008.11.011Halogenated sesquiterpenes and non-halogenated linear C15-acetogenins from the marine red alga Laurencia composita and their chemotaxonomic significance
resolves10.1002/hlca.201000158Sesquiterpenes and Other Metabolites from the Marine Red Alga <i>Laurencia composita</i> (Rhodomelaceae)
resolves10.1021/ja054316o7-<i>e</i><i>ndo</i> Radical Cyclizations Catalyzed by Titanocene(III). Straightforward Synthesis of Terpenoids with Seven-Membered Carbocycles
resolves10.1016/S0040-4039(01)83025-2Laurencenyne, a plausible precursor of various nonterpenoid C15-compounds, and neolaurencenyne from the red alga
resolves10.1016/S0040-4039(00)87136-1Isolation and structures of -laurencenyne, a possible precursor of the C15 halogenated cyclic ethers, and -neolaurencenyne from
resolves10.1016/S0040-4020(01)87533-5Isolation of (10R,11R)-(+)-squalene-10,11-epoxide from the red alga laurencia okamurai and its enantioselective synthesis
resolves10.1016/S0040-4039(00)93984-4Marine sterols. 23. 2a-oxa-2-oxo-5α-hydroxy-3,4-dinorcholestane from the arabian sea red alga laurencia obtusa
resolves10.1021/np50106a006New C<sub>15</sub> Acetogenins and Sesquiterpenes from the Red Alga Laurencia sp. cf. L. gracilis
resolves10.1021/np970181r<i>Laurencia rigida</i>: Chemical Investigations of Its Antifouling Dichloromethane Extract
resolves10.1246/cl.1983.29LAUREACETAL-C, AN UNUSUAL SECOCHAMIGRANE SESQUITERPENE FROM THE RED ALGA <i>LAURENCIA NIPPONICA</i> YAMADA
resolves10.1023/A:1008037706596Growth and the content of laurinterol and debromolaurinterol in Laurencia okamurae (Ceramiales, Rhodophyta)
resolves10.3390/md10122817Sesquiterpene and Acetogenin Derivatives from the Marine Red Alga Laurencia okamurai
resolves10.1002/hlca.200590074Cuparene‐Derived Sesquiterpenes from the Chinese Red Alga <i>Laurencia okamurai</i> Y<scp>amada</scp>
resolves10.1021/np0503810A Laurane Sesquiterpene and Rearranged Derivatives from the Chinese Red Alga <i>Laurencia </i><i>o</i><i>kamurai</i> Yamada
resolves10.1021/ja00288a048Stereocontrolled syntheses of (E)- and (Z)-.gamma.-bisabolene 8,9-epoxide
resolves10.1246/cl.2010.366Papillamide, a Novel Fatty Acid Amide from the Red Alga <i>Laurencia papillosa</i>
resolves10.1002/hlca.200890137Squalene‐Derived Triterpene Polyethers from the Red Alga <i>Laurencia omaezakiana</i>
resolves10.1021/np049753fLaurenditerpenol, a New Diterpene from the Tropical Marine Alga <i>Laurencia </i><i>i</i><i>ntricata</i> that Potently Inhibits HIF-1 Mediated Hypoxic Signaling in Breast Tumor Cells
resolves10.1021/ja990154iEffective Combination of Two-Directional Synthesis and Rhenium(VII) Chemistry: Total Synthesis of meso Polyether Teurilene
resolves10.1002/anie.200805857Total Synthesis and Determination of the Absolute Configuration of (+)‐Omaezakianol
resolves10.1039/p19930002329Chiral cyclobutanones as versatile synthons: the first enantioselective total synthesis of (+)-laurene
resolves10.1016/S0040-4039(00)01484-2A short synthesis of (±)-laurene: mechanistic reinvestigation in palladium-catalyzed cycloreductions of 1,6-enynes
resolves10.3390/md9112220New Polyether Triterpenoids from Laurencia viridis and Their Biological Evaluation
resolves10.1071/CH9960019Parguerenes Revisited: New Brominated Diterpenes From the Southern Australian Marine Red Alga
<i>Laurencia Filiformis</i>
resolves10.1016/S0040-4039(00)88262-3The isolation and structure determination of chilenone A, a putative dimer of 2-methyl-3(2H)-furanone from the marine alga
resolves10.1016/S0040-4039(00)96850-3Further structural studies on the 2-methyl-3(2H)-furanone derived metabolites of the marine alga Laurencia chilensis
resolves10.1016/S0040-4020(01)81528-3A radical cyclisation based strategy to cuparenoids; synthesis of (±)-α-cuparenone, (±)-epilaurene and laurenes
resolves10.1016/0040-4020(78)89006-1The brasilenols, rearranged sesquiterpene alcohols isolated from the marine opisthobranch aplysia brasiliana
resolves10.1021/jo00402a039Sesquiterpenoids from the Hawaiian marine alga Laurencia nidifica. 7. (+)-Selina-4,7(11)-diene
resolves10.1246/bcsj.52.3352Halogenated and Non-halogenated Aromatic Sesquiterpenes from the Red Algae <i>Laurencia okamurai</i> Yamada
resolves10.1246/cl.1980.1267(<i>E</i>)-γ-BISABOLEN-8,9-EPOXIDE AND ISOCYCLOEUDESMOL, TWO NEW SESQUITERPENOIDS FROM THE MARINE RED ALGA <i>LAURENCIA NIPPONICA</i> YAMADA1)
resolves10.1246/bcsj.55.1561Six New Sesquiterpenoids from the Red Alga <i>Laurencia nipponica</i> Yamada
resolves10.1016/S0040-4039(00)94885-8Teurilene and thyrsiferyl 23-acetate, meso and remarkably cytotoxic compounds from the marine red alga laurencia obtusa (hudson) lamouroux
resolves10.1246/bcsj.60.3793(<i>E</i>)-2-Tridecyl-2-heptadecenal, an Unusual Metabolite from the Red Alga <i>Laurencia</i> Species
resolves10.1246/bcsj.60.3795Majusculone, a Novel Norchamigrane-Type Metabolite from the Red Alga <i>Laurencia majuscula</i> Harvey
resolves10.1246/cl.1990.155A New Naturally Occurring Racemic Compound from the Marine Red Alga <i>Laurencia obtusa</i> (Hudson) Lamouroux
resolves10.1021/np030176pBrominated Sesquiterpenes from the Red Alga <i>Laurencia </i><i>o</i><i>btusa</i>
resolves10.1016/S0040-4039(00)76841-9Revised structure of a brasilane-type sesquiterpene isolated from the red alga Laurencia implicata and its absolute configuration
resolves10.1021/cr9002215Halogenated Organic Molecules of Rhodomelaceae Origin: Chemistry and Biology
resolves10.1021/np50070a012Tropical Marine Algae, VII. The Chemical Composition of Marine Algae from North Queensland Waters
resolves10.1021/np50076a016New Sesquiterpenes and C<sub>15</sub> Acetogenins from the Marine Red Alga Laurencia implicata
resolves10.1021/np020274vThree New Sesquiterpenes from the Red Alga <i>Laurencia perforata</i>
resolves10.1021/ol100213eA Short Total Synthesis of (+)-Omaezakianol via an Epoxide-Initiated Cationic Cascade Reaction
The 7 references without a DOI — listed, not checked
no DOI — not checkedKigoshi H, Ojika M, Shizuri Y, Niwa H, Yamada K (1982a) (10R,11R)-(+)-Squalene-10,11-epoxide: isolation from Laurencia okamurai and the asymmetric synthesis. Tetrahedron Lett 23:5413–5414
no DOI — not checkedMakhanu DS, Yokoyama M, Miono T, Maesato T, Maedomari M, Wisespongpand P, Kuniyoshi M (2006) New sesquiterpenes from the Okinawan red alga Laurencia luzonensis. Bull Fac Sci Univ Ryukyus 81:115–120
no DOI — not checkedMao SC, Guo YW (2010) Sesquiterpenes from Chinese red alga Laurencia okamurai. Chin J Nat Med 8:321–325
no DOI — not checkedSun J, Han LJ, Shi DY, Fan X, Wang SJ, Li S, Yang YC, Shi JG (2005a) Sesquiterpenes from red alga Laurencia tristicha. Chin Chem Lett 16:1611–1614
no DOI — not checkedXu XH, Lu JH, Yao GM, Li YM (2001) Studies on the chemical constituent of the alga Laurencia majuscula. Nat Prod Res Dev 13(5):5–8
no DOI — not checkedXu SH, Yang XY, Liao XJ, Guo SH (2005) A new pentahydroxyceramide from Laurencia cartilaginea. J Chin Med Mater 28:1067–1069
no DOI — not checkedZhong YL, Su JY, Zeng LM, Yan SJ, Luo BH (1996) Studies on the chemical constituents of Laurencia karlae collected from the South China Sea. Chem J Chin Univ 17:249–251
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