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A sesquiterpene thiocyanate and three sesquiterpene isothiocyanates from the sponge Trachyopsis aplysinoides
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inferred← citeshttps://doi.org/10.2139/ssrn.4057421openalex-extracted
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inferred← citeshttps://doi.org/10.1002/adsc.201700015openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.201500453openalex-snapshot
N‐Bromosuccinimide‐Mediated Thiocyanation of Cyclohexene‐Fused Isoxazoline N‐Oxides
inferred← citeshttps://doi.org/10.1002/ajoc.202200007openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.200417290openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202100278openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202300148openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.202401180openalex-snapshot
Visible‐Light‐Induced Mpg‐C3N4 Catalyzed C(sp2)−H Thiocyanation of Ketene Dithioacetals
inferred← citeshttps://doi.org/10.1002/hlca.200490263openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-7091-6331-3_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12272-012-0503-2openalex-snapshot
Bioactive cadinane-type compounds from the soft coral Sinularia scabra
inferred← citeshttps://doi.org/10.1016/0020-1693(96)84700-1openalex-snapshot
Vanadium bromoperoxidase-catalyzed oxidation of thiocyanate by hydrogen peroxide
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00295-5openalex-snapshot
Total synthesis of (±)-halipanicine
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00481-4openalex-snapshot
New antifouling sesquiterpenes from four nudibranchs of the family Phyllidiidae
inferred← citeshttps://doi.org/10.1016/0040-4039(91)80501-vopenalex-snapshot
Two new sesquiterpene isonitriles from the nudibranch, phyllida pustulosa
inferred← citeshttps://doi.org/10.1016/0305-1978(92)90082-oopenalex-snapshot
Chemotaxonomy of Agelas (Porifera: Demospongiae)
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.06.011openalex-snapshot
Survey of marine natural product structure revisions: A synergy of spectroscopy and chemical synthesis
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.12.080openalex-snapshot
Natural product-based synthesis of novel anti-infective isothiocyanate- and isoselenocyanate-functionalized amphilectane diterpenes
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.04.039openalex-snapshot
Synthesis and preliminary evaluation of 3-thiocyanato-1H-indoles as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.10.003openalex-snapshot
New sesquiterpenoid isonitriles from three species of phyllidid nudibranchs
inferred← citeshttps://doi.org/10.1016/j.tet.2006.08.070openalex-snapshot
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
inferred← citeshttps://doi.org/10.1016/j.tet.2016.05.060openalex-snapshot
Sesquiterpene isocyanides, isothiocyanates, thiocyanates, and formamides from the Thai sponge Halichondria sp.
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153809openalex-snapshot
An efficient synthesis of 4-Thiocyanato anilines using benzyltrimethylammonium dichloroiodate and ammonium thiocyanate in DMSO:H2O
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96120-4openalex-snapshot
Novel marine sponge derived amino acids 13. Additional psammaplin derivatives from Psammaplysilla purpurea
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)61785-9openalex-snapshot
Two sesquiterpene isocyanides and a sesquiterpene thiocyanate from the marine sponge Acanthella cf. cavernosa and the Nudibranch Phyllidia ocellata
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74680-6openalex-snapshot
Facile syntheses of some trans-hydroazulenes by means of electrochemical methodology coupled with base-catalyzed fragmentation reaction
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)93475-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01668-9openalex-snapshot
Restructuring α-pinene: novel entry into diverse polycarbocyclic frameworks
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)00121-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01149-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02522-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1099-4831(05)61002-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80010-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1572-5995(01)80023-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1572-5995(03)80151-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00502openalex-snapshot
Tricyclic Sesquiterpenes from Marine Origin
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02834openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ar00022a001openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo0102765openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np070156dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np300439eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b300664fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/b302359copenalex-snapshot
Marine isocyanides and related natural products ? structure, biosynthesis and ecology
inferred← citeshttps://doi.org/10.1039/d1qo01710aopenalex-snapshot
Oxidative thiocyanation of allylic alcohols: an easy access to allylic thiocyanates with K 2 S 2 O 8 and NH 4 SCN
inferred← citeshttps://doi.org/10.1039/d3ob00438dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3ob01898aopenalex-snapshot
Copper-catalyzed thiocyanation of cyclobutanone oxime esters using ammonium thiocyanate
inferred← citeshttps://doi.org/10.1080/00397910801997744openalex-snapshot
Triphosgene: An Efficient Catalyst for Synthesis of Isothiocyanates
inferred← citeshttps://doi.org/10.1080/14786410802587073openalex-snapshot
New synthesis of nematocidal natural products dithiocynates thiocyanatin A and 1,8,16-trihydroxyhexadecane
inferred← citeshttps://doi.org/10.1246/bcsj.72.85openalex-snapshot
Synthesis of Medium-Sized Bicyclic Compounds by Intramolecular Cyclization of Cyclic β-Keto Radicals Generated from Cyclopropanols Using Manganese(III) Tris(pyridine-2-carboxylate) and Its Application to Total Synthesis of 10-Isothiocyanatoguaia-6-ene
inferred← citeshttps://doi.org/10.1246/cl.1994.1697openalex-snapshot
Total Synthesis of 10-Isothiocyanatoguaia-6-ene
inferred← citeshttps://doi.org/10.3390/chemistry6030027openalex-snapshot
An Efficient and Eco-Friendly Procedure for Electrophilic Thiocyanation of Anilines and 1-(Substituted benzylidene)-2-phenyl Hydrazines
inferred← citeshttps://doi.org/10.3390/md14010016openalex-snapshot
Marine Isonitriles and Their Related Compounds
inferred← citeshttps://doi.org/10.3390/md17050301openalex-snapshot
Renieramycin T Induces Lung Cancer Cell Apoptosis by Targeting Mcl-1 Degradation: A New Insight in the Mechanism of Action
inferred← citeshttps://doi.org/10.3390/md23050220openalex-snapshot
The Enigma of Sponge-Derived Terpenoid Isothiocyanate–Thiocyanate Pairs: A Biosynthetic Proposal
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.74.689openalex-snapshot
Total Synthesis of Natural Antifouling Products
inferred← citeshttps://doi.org/10.58837/chula.the.2019.423openalex-snapshot
Anti-cancer effects of renieramycin T on human non-small cell lung cancer cells
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