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A new diisocyanide of novel ring structure from a sponge

https://doi.org/10.1021/ja00429a053
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113512zenodo-depositor-declared
Kalihiacyloxyamides A-H, α-acyloxy amide substituted kalihinane diterpenes isolated from the sponge Acanthella cavernosa collected in the South China Sea
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod019openalex-snapshot
Porifera (Sponges)–1
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod192openalex-snapshot
Porifera (Sponges)–2
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod193openalex-snapshot
Porifera (Sponges)–3
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/ange.201603581openalex-snapshot
A Formal Enantiospecific Synthesis of 7,20‐Diisocyanoadociane
inferred← citeshttps://doi.org/10.1002/ange.201906834openalex-snapshot
Concise Synthesis of the Antiplasmodial Isocyanoterpene 7,20‐Diisocyanoadociane
inferred← citeshttps://doi.org/10.1002/ange.201913645openalex-snapshot
Fragmentverknüpfungen in der Totalsynthese – Bildung von C‐C‐Bindungen über intermediäre Carbanionen oder freie Radikale
inferred← citeshttps://doi.org/10.1002/anie.201603581openalex-snapshot
A Formal Enantiospecific Synthesis of 7,20‐Diisocyanoadociane
inferred← citeshttps://doi.org/10.1002/anie.201906834openalex-snapshot
Concise Synthesis of the Antiplasmodial Isocyanoterpene 7,20‐Diisocyanoadociane
inferred← citeshttps://doi.org/10.1002/anie.201913645openalex-snapshot
Fragment Coupling Reactions in Total Synthesis That Form Carbon–Carbon Bonds via Carbanionic or Free Radical Intermediates
inferred← citeshttps://doi.org/10.1002/chin.197638358openalex-snapshot
ChemInform Abstract: A NEW DIISOCYANIDE OF NOVEL RING STRUCTURE FROM A SPONGE
inferred← citeshttps://doi.org/10.1002/hlca.19790620742openalex-snapshot
Defense Allomones of the Nudibranch Phyllidia varicosa Lamarck 1801
inferred← citeshttps://doi.org/10.1002/mrc.1260330814openalex-snapshot
1H (300 MHz) and 13 C NMR spectral assignments for diisocyanoadociane
inferred← citeshttps://doi.org/10.1007/978-1-4899-4513-6_4openalex-snapshot
Diterpenoids
inferred← citeshttps://doi.org/10.1007/978-3-7091-6331-3_1openalex-snapshot
Naturally Occurring Isocyano/Isothiocyanato and Related Compounds*
inferred← citeshttps://doi.org/10.1007/bf02536153openalex-snapshot
Terpenes in sponge cell membranes: Cell separation and membrane fractionation studies with the tropical marine spongeAmphimedon sp.
inferred← citeshttps://doi.org/10.1007/bf02578249openalex-snapshot
The distribution of brominated long‐chain fatty acids in sponge and symbiont cell types from the tropical marine spongeAmphimedon terpenensis
inferred← citeshttps://doi.org/10.1007/bfb0034370openalex-snapshot
Marine isocyano compounds
inferred← citeshttps://doi.org/10.1016/0305-0491(88)90145-9openalex-snapshot
Isoprenoid biosynthesis in a marine sponge of the Amphimedon genus: Incorporation studies with [1-14C] acetate, [4-14C] cholesterol and [2-14C] mevalonate
inferred← citeshttps://doi.org/10.1016/0305-0491(90)90274-wopenalex-snapshot
Biosynthesis of marine isocyanoterpenoids in sponges
inferred← citeshttps://doi.org/10.1016/b978-0-12-624002-3.50010-3openalex-snapshot
Diterpenoids
inferred← citeshttps://doi.org/10.1016/j.tet.2005.05.102openalex-snapshot
Structural and stereochemical revision of isocyanide and isothiocyanate amphilectenes from the Caribbean marine sponge Cribochalina sp.
inferred← citeshttps://doi.org/10.1016/s0014-5793(98)00736-4openalex-snapshot
Isolation and characterization of adociavirin, a novel HIV‐inhibitory protein from the sponge Adocia sp.1
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00169-5openalex-snapshot
Sinulobatins A ∼ D, new amphilectane-type diterpenoids from the Japanese soft coral Sinularia nanolobata
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)71200-7openalex-snapshot
New diterpene isocyanides from a sponge
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)91682-4openalex-snapshot
Two New Diterpene Isocyanides from a Sponge of the Family Adocidae
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91295-xopenalex-snapshot
Novel bisabolene-type sesquiterpenoids with a conjugated diene isolated from the okinawan sea sponge theonella cf. swinhoei
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00567-5openalex-snapshot
Advanced precursors in marine biosynthetic study: The biosynthesis of diisocyanoadociane in Amphimedon terpenensis
inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80010-1openalex-snapshot
Cyanide and thiocyanate-derived functionality in marine organisms - structures, biosynthesis and ecology
inferred← citeshttps://doi.org/10.1016/s1874-6004(08)80006-8openalex-snapshot
Chapter 2 A formal total synthesis of the marine diterpenoid, diisocyanoadociane
inferred← citeshttps://doi.org/10.1021/acs.analchem.6c03693openalex-snapshot
Reactivity-Guided Detection Strategies for Isocyanide Natural Products Reveal Acid-Induced Hazimycin Artifacts
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00143openalex-snapshot
Medicinal Chemistry of Isocyanides
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01295openalex-snapshot
The Paradox of Antimalarial Terpenoid Isonitrile Biosynthesis Explained. Proposal of Cyanoformate as an NC Delivery Vector
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00914openalex-snapshot
Nitrogen-Functionalized Amphilectane-Type Diterpenoids with Anti-HBV Activity from the Okinawan Marine Sponge Stylissa sp.
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02700openalex-snapshot
Evolution of a Short and Stereocontrolled Synthesis of (+)-7,20-Diisocyanoadociane
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00448openalex-snapshot
General Approaches to Structurally Diverse Isocyanoditerpenes
inferred← citeshttps://doi.org/10.1021/jo401846mopenalex-snapshot
Two Rare-Class Tricyclic Diterpenes with Antitubercular Activity from the Caribbean Sponge Svenzea flava. Application of Vibrational Circular Dichroism Spectroscopy for Determining Absolute Configuration
inferred← citeshttps://doi.org/10.1021/jo952015zopenalex-snapshot
Novel Potent Antimalarial Diterpene Isocyanates, Isothiocyanates, and Isonitriles from the Tropical Marine Sponge Cymbastela hooperi
inferred← citeshttps://doi.org/10.1021/ol061228fopenalex-snapshot
A Formal Total Synthesis of the Marine Diterpenoid Diisocyanoadociane
inferred← citeshttps://doi.org/10.1021/ol502205mopenalex-snapshot
Investigations into an Anionic Oxy-Cope/Transannular Conjugate Addition Approach to 7,20-Diisocyanoadociane
inferred← citeshttps://doi.org/10.1039/np9971400259openalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1071/ch10073openalex-snapshot
Marine Pharmacology in Australia. The Roche Research Institute at Dee Why, New South Wales, 1974–81
inferred← citeshttps://doi.org/10.1071/hr09013openalex-snapshot
The Roche Research Institute of Marine Pharmacology, 1974–1981: Searching for Drug Leads from Australian Marine Organisms
inferred← citeshttps://doi.org/10.1080/01961778608082487openalex-snapshot
Organic Sulfur Compounds from Marine Organisms
inferred← citeshttps://doi.org/10.1107/s0108768198006570openalex-snapshot
Low-temperature crystallization and structure determination of N-(trifluoromethyl)formamide, N-(2,2,2-trifluoroethyl)formamide and 2,2,2-trifluoroethyl isocyanide
inferred← citeshttps://doi.org/10.1246/cl.2011.246openalex-snapshot
A Formal Synthesis of Antimalarial Diterpenoid 7,20-Diisocyanoadociane
inferred← citeshttps://doi.org/10.3390/md14010016openalex-snapshot
Marine Isonitriles and Their Related Compounds
inferred← citeshttps://doi.org/10.3390/md23050220openalex-snapshot
The Enigma of Sponge-Derived Terpenoid Isothiocyanate–Thiocyanate Pairs: A Biosynthetic Proposal
inferred← citeshttps://doi.org/10.56253/jaser.2.1.2021.1-33openalex-snapshot
An overview of Isocyanide
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