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A New 1,2-Dihydroisoquinoline from the Sponge Petrosia similis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1021/jo00241a050openalex-snapshot
Bisannelation with a benzo[1,2-c:4,5-c']difuran equivalent: a new route to linear acene derivatives
inferredcites →https://doi.org/10.1021/np9802015openalex-snapshot
Five New Polyacetylenes from a Sponge of the Genus Petrosia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4673837openalex-extracted
Rhenium-Catalyzed Synthetic Method of 1,2-Dihydroisoquinolines and Isoquinolines
inferred← citeshttps://doi.org/10.1002/adsc.200900442openalex-snapshot
Multicatalytic Tandem Reactions of 2‐Alkynylbenzaldoximes with Isocyanides
inferred← citeshttps://doi.org/10.1002/adsc.201000080openalex-snapshot
Three‐Component Reactions of 2‐Alkynylbenzaldoximes and α,β‐Unsaturated Carbonyl Compounds with Bromine or Iodine Monochloride
inferred← citeshttps://doi.org/10.1002/asia.202000322openalex-snapshot
Metal‐Free Facile Synthesis of Multisubstituted 1‐Aminoisoquinoline Derivatives with Dual‐State Emissions
inferred← citeshttps://doi.org/10.1002/chem.201504914openalex-snapshot
Rhodium(II)‐Catalyzed and Thermally Induced Intramolecular Migration of N‐Sulfonyl‐1,2,3‐triazoles: New Approaches to 1,2‐Dihydroisoquinolines and 1‐Indanones
inferred← citeshttps://doi.org/10.1002/jhet.2241openalex-snapshot
One‐Pot Domino Synthesis of 3‐Amino‐1,2‐dihydroisoquinolines
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_11openalex-snapshot
Typification of Chemical Compounds of Marine Sponge Metabolites
inferred← citeshttps://doi.org/10.1016/bs.alkal.2025.12.001openalex-snapshot
Renieramycin-type bis-1,2,3,4-tetrahydroisoquinoline marine natural products
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.06.060openalex-snapshot
Crystal structures, phosphorescent and magnetic properties of novel 1,2-dihydroisoquinoline radicals
inferred← citeshttps://doi.org/10.1016/j.tet.2004.02.071openalex-snapshot
Chemistry of renieramycins. Part 6: Transformation of renieramycin M into jorumycin and renieramycin J including oxidative degradation products, mimosamycin, renierone, and renierol acetate
inferred← citeshttps://doi.org/10.1016/j.tet.2008.12.038openalex-snapshot
Synthesis of 1,2-dihydroisoquinolin-1-ylphosphonates via three-component reactions of 2-(2-formylphenyl)ethanone, amine, and diethyl phosphite
inferred← citeshttps://doi.org/10.1016/j.tet.2010.08.052openalex-snapshot
Three-component reaction of N′-(2-alkynylbenzylidene)hydrazide, α,β-unsaturated carbonyl compound, with bromine
inferred← citeshttps://doi.org/10.1016/j.tet.2010.12.005openalex-snapshot
An efficient route to diverse H-pyrazolo[5,1-a]isoquinolines via sequential multi-component/cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2011.01.048openalex-snapshot
Library construction of 1-(1H-imidazol-1-yl)-1,2-dihydroisoquinolines via three-component reaction of 2-alkynylbenzaldehyde, amine, and imidazole
inferred← citeshttps://doi.org/10.1016/j.tet.2011.04.063openalex-snapshot
An expeditious approach to 1-aminoisoquinolines via an unexpected reaction of 2-alkynylbenzaldoxime, carbodiimide, with bromine
inferred← citeshttps://doi.org/10.1016/j.tet.2012.08.039openalex-snapshot
One-pot two-step synthesis of 1-position arylated 1,3-disubstituted isoquinoline N-oxides
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.026openalex-snapshot
Facile assembly of 1-(4-haloisoquinolin-1-yl)ureas via a reaction of 2-alkynylbenzaldoxime, carbodiimide, and halide in water
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132576openalex-snapshot
A review of the synthesis of 1,2-dihydroisoquinoline, [2,1-a] isoquinoline and [5,1-a] isoquinoline since 2006
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133491openalex-snapshot
Advances and applications of 2-alkynylbenzaldoxime as a valuable synthetic framework for synthesizing N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133854openalex-snapshot
Rhenium-catalyzed synthetic method of 1,2-dihydroisoquinolines and isoquinolines by the intramolecular cyclization of 2-alkynylaldimines or 2-alkynylbenzylamines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.02.143openalex-snapshot
AgOTf-catalyzed one-pot reaction of 2-alkynylbenzaldehyde, amine, and sodium borohydride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.121openalex-snapshot
Tandem cyclization-[3+3] cycloaddition reactions of 2-alkynylbenzaldoxime: synthesis of fused 1,2-dihydroisoquinolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.11.006openalex-snapshot
Highly efficient electrophilic cyclization of N′-(2-alkynylbenzylidene)hydrazides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.03.159openalex-snapshot
Synthesis of polysubstituted 1,2-dihydroisoquinolines via a CuI-catalyzed arylation/condensation cascade process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.013openalex-snapshot
Lewis acid-catalyzed reactions of N′-(2-alkynylbenzylidene)hydrazides with diethyl phosphite
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.106openalex-snapshot
Multicatalytic synthesis of 1,2-dihydroisoquinolin-1-ylphosphonates via a tandem four-component reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155844openalex-snapshot
Tandem Mizoroki-Heck arylation and Aza-Michael reaction: A rapid access to 1,3-Disubstituted-1,2-dihydroisoquinoline derivatives
inferred← citeshttps://doi.org/10.1021/cc9001263openalex-snapshot
Synthesis of 1-(1H-Indol-3-yl)-1,2-dihydroisoquinolines via AgOTf-Catalyzed Three-Component Reactions of 2-Alkynylbenzaldehydes, Amines, and Indoles
inferred← citeshttps://doi.org/10.1021/co1000794openalex-snapshot
Solution-Phase Parallel Synthesis of a Diverse Library of 1,2-Dihydroisoquinolines
inferred← citeshttps://doi.org/10.1021/jacs.4c10019openalex-snapshot
Palladium-Catalyzed Asymmetric Larock Isoquinoline Synthesis to Access Axially Chiral 3,4-Disubstituted Isoquinolines
inferred← citeshttps://doi.org/10.1021/jo4009639openalex-snapshot
On Water: Silver-Catalyzed Domino Approach for the Synthesis of Benzoxazine/Oxazine-Fused Isoquinolines and Naphthyridines from o-Alkynyl Aldehydes
inferred← citeshttps://doi.org/10.1021/jo802076kopenalex-snapshot
Tandem Electrophilic Cyclization−[3+2] Cycloaddition−Rearrangement Reactions of 2-Alkynylbenzaldoxime, DMAD, and Br2
inferred← citeshttps://doi.org/10.1021/ol101988qopenalex-snapshot
Efficient Generation of Biologically Active H-Pyrazolo[5,1-a]isoquinolines via Multicomponent Reaction
inferred← citeshttps://doi.org/10.1021/ol200629yopenalex-snapshot
Silver Triflate Catalyzed Reaction of 2-Alkynylbenzaldoxime with Aryne
inferred← citeshttps://doi.org/10.1021/ol300901xopenalex-snapshot
An Unexpected Silver Triflate Catalyzed Reaction of 2-Alkynylbenzaldehyde with 2-Isocyanoacetate
inferred← citeshttps://doi.org/10.1021/ol402996xopenalex-snapshot
Cu-Catalyzed 1,2-Dihydroisoquinolines Synthesis from o-Ethynyl Benzacetals and Sulfonyl Azides
inferred← citeshttps://doi.org/10.1039/b904498aopenalex-snapshot
AgOTf-catalyzed tandem reaction of N′-(2-alkynylbenzylidene)hydrazide with alkyne
inferred← citeshttps://doi.org/10.1039/b913409copenalex-snapshot
Multicatalytic tandem reaction of N′-(2-alkynylbenzylidene)hydrazide with indole
inferred← citeshttps://doi.org/10.1039/c0cc01207fopenalex-snapshot
Silver triflate and N-heterocyclic carbene co-catalyzed reaction of N′-(2-alkynylbenzylidene)hydrazide, methanol with α,β-unsaturated aldehyde
inferred← citeshttps://doi.org/10.1039/c2ra01056aopenalex-snapshot
Recent developments in solvent-free multicomponent reactions: a perfect synergy for eco-compatible organic synthesis
inferred← citeshttps://doi.org/10.1039/c3ra42730gopenalex-snapshot
Generation of diverse isoquinoline N-oxides in an aqueous system
inferred← citeshttps://doi.org/10.1039/c4ob02036gopenalex-snapshot
An expedient approach to 1,2-dihydroisoquinoline derivatives via cobalt catalysed 6-endo dig cyclization followed by Mannich condensation of o-alkynylarylaldimines
inferred← citeshttps://doi.org/10.1039/c6cc03650copenalex-snapshot
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations
inferred← citeshttps://doi.org/10.1039/d0ob01517bopenalex-snapshot
Synthesis of organoselenyl isoquinolinium imides via iron( iii ) chloride-mediated tandem cyclization/selenation of N ′-(2-alkynylbenzylidene)hydrazides and diselenides
inferred← citeshttps://doi.org/10.1039/d0qo00279hopenalex-snapshot
Transition metal-catalyzed coupling of heterocyclic alkenes via C–H functionalization: recent trends and applications
inferred← citeshttps://doi.org/10.1039/d2ob00275bopenalex-snapshot
Synthesis of functionalized 1-aminoisoquinolines through cascade three-component reaction of ortho -alkynylbenzaldoximes, 2 H -azirines, and electrophiles
inferred← citeshttps://doi.org/10.1080/14786419.2023.2175359openalex-snapshot
Two new sarasinosides from marine sponge Petrosia nigricans
inferred← citeshttps://doi.org/10.1177/1934578x0800301119openalex-snapshot
New Purine Derivatives from the Marine Sponge Petrosia nigricans
inferred← citeshttps://doi.org/10.1177/1934578x1300800905openalex-snapshot
Biscembranoids from the Marine Sponge Petrosia Nigricans
inferred← citeshttps://doi.org/10.1246/bcsj.20190301openalex-snapshot
Catalytic Synthesis of Isoquinolines via Intramolecular Migration of N-Aryl Sulfonyl Groups on 1,5-Yne-Imines
inferred← citeshttps://doi.org/10.1246/cl.180200openalex-snapshot
Synthesis of 1,2-Dihydroisoquinolines via Rhenium-catalyzed Tandem Cyclization and Nucleophilic Addition of 2-(1-Alkynyl)arylaldimines
inferred← citeshttps://doi.org/10.1248/bpb.26.1498openalex-snapshot
Anti-HIV Active Petrosins from the Marine Sponge Petrosia similis1)
inferred← citeshttps://doi.org/10.1248/cpb.52.282openalex-snapshot
Chemistry of Renieramycins. Part 4. Synthesis of a Simple Natural Marine Product, 6-Hydroxy-7-methoxyisoquinolinemethanol
inferred← citeshttps://doi.org/10.3390/md15030054openalex-snapshot
Sterols from Thai Marine Sponge Petrosia (Strongylophora) sp. and Their Cytotoxicity
inferred← citeshttps://doi.org/10.3390/md19030122openalex-snapshot
Secondary Metabolites from the Marine Sponges of the Genus Petrosia: A Literature Review of 43 Years of Research
inferred← citeshttps://doi.org/10.3390/molecules29122917openalex-snapshot
Synthesis of Substituted 1,2-Dihydroisoquinolines by Palladium-Catalyzed Cascade Cyclization–Coupling of Trisubstituted Allenamides with Arylboronic Acids
inferred← citeshttps://doi.org/10.3987/com-17-13694openalex-snapshot
Copper Accelerated One-Pot Sequential Tandem Synthesis of Tetrahydropurinoisoquinoline Derivatives
inferred← citeshttps://doi.org/10.3987/rev-13-781openalex-snapshot
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