A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
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1α,25(OH)2-3-epi-vitamin D3, a natural physiological metabolite of vitamin D3: its synthesis, biological activity and crystal structure with its receptorA Regioselective Synthesis of the Dephospho DIthiolene Protected Molybdopterin.Alkyne metathesis: development of a novel molybdenum-based catalyst system and its application to the total synthesis of epothilone A and C.Non-natural acetogenin analogues as potent Trypanosoma brucei inhibitors.Total Synthesis and Structural Revision of Antibiotic CJ-16,264.Elucidating Structure-Bioactivity Relationships of Methyl-Branched Alkanes in the Contact Sex Pheromone of the Parasitic Wasp Lariophagus distinguendusEvolution of a Unified Strategy for Complex Sesterterpenoids: Progress toward Astellatol and the Total Synthesis of (-)-Nitidasin.Asymmetric synthesis of naturally occurring spiroketals.Highly stereoselective total synthesis of fully hydroxy-protected mycolactones A and B and their stereoisomerization upon deprotectionTotal synthesis of (-)-spinosyn A.Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.Chemical architecture and applications of nucleic acid derivatives containing 1,2,3-triazole functionalities synthesized via click chemistry.Advances in the total synthesis of biologically important callipeltosides: a review.Preparation of carbon nanomaterials from molecular precursors.Ethynylglycine synthon, a useful precursor for the synthesis of biologically active compounds: an update: part I: preparations of ethynylglycine synthon.Making a Long Journey Short: Alkyne Functionalization of Natural Product Scaffolds.Advances in the synthesis of α-quaternary α-ethynyl α-amino acids.A Highly Reactive Geminal P/B Frustrated Lewis Pair: Expanding the Scope to C-X (X=Cl, Br) Bond Activation.Total synthesis of (-)-zampanolide and structure-activity relationship studies on (-)-dactylolide derivatives.Enantiospecific Alkynylation of Alkylboronic Esters.5',6'-nucleoside phosphonate analogues architecture: synthesis and comparative evaluation towards metabolic enzymes.Tetrahydrofuran amino acid-containing gramicidin S analogues with improved biological profiles.The cobalt way to angucyclinones: asymmetric total synthesis of the antibiotics (+)-rubiginone B2, (-)-tetrangomycin, and (-)-8-O-methyltetrangomycin.Ring expansion of alkynyl cyclopropanes to highly substituted cyclobutenes via a N-sulfonyl-1,2,3-triazole intermediate.Callipeltosides A, B and C: Total Syntheses and Structural Confirmation.Electron transfer through molecular bridges between reducible pentakis(thiophenyl)benzene subunits.Synthesis of azahelicene N-oxide by palladium-catalyzed direct C-H annulation of a pendant (Z)-bromovinyl side chain.Efficient synthesis of highly functionalized indazoles and 2,3-dihydro-1,2-benzisoxazoles by reaction of stable Fischer dienyl carbenes and isocyanides.The total synthesis of the annonaceous acetogenin, muricatetrocin C.Total synthesis of plakortide E and biomimetic synthesis of plakortone B.Highly efficient stereocontrolled total synthesis of the polyfunctional carotenoid peridinin.Concise total synthesis of the aporphine alkaloid 7,7'-bisdehydro-O-methylisopiline by an InCl3 mediated cycloisomerization reaction.Open-chain carbocyclic analogs of adenosine with dihalovinyl unit as potential inhibitors of S-adenosyl-L-homocysteine hydrolase.The Ireland-Claisen rearrangement as a probe for the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group.The first total synthesis of cytopiloyne, an anti-diabetic, polyacetylenic glucoside.Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of furanyl (gamma)- and pyranyl (delta)-lactols.Synthesis of phenanthrenes and polycyclic heteroarenes by transition-metal catalyzed cycloisomerization reactions.Synthesis and determination of the absolute configuration of fugomycin and desoxyfugomycin: CD spectroscopy and fungicidal activity of butenolides.Regio- and stereochemical studies on the nitroso-Diels-Alder reaction with 1,2-disubstituted dienes.Synthesis of the pluramycins 2: total synthesis and structure assignment of saptomycin B.
P2860
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P2860
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
description
1972 nî lūn-bûn
@nan
1972 թուականին հրատարակուած գիտական յօդուած
@hyw
1972 թվականին հրատարակված գիտական հոդված
@hy
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
name
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@ast
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@en
type
label
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@ast
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@en
prefLabel
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@ast
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@en
P1433
P1476
A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)
@en
P2093
P.L. Fuchs
P304
P356
10.1016/S0040-4039(01)94157-7
P577
1972-01-01T00:00:00Z