about
Synthesis and stereochemical determination of an antiparasitic pseudo-aminal type monoterpene indole alkaloidHigh resolution crystal structures of triosephosphate isomerase complexed with its suicide inhibitors: The conformational flexibility of the catalytic glutamate in its closed, liganded active siteStructural and mechanistic studies on carboxymethylproline synthase (CarB), a unique member of the crotonase superfamily catalyzing the first step in carbapenem biosynthesisDFT study of the mechanism of the reaction of aminoguanidine with methylglyoxalThe Problem of Origins and Origins of the Problem: Influence of Language on Studies Concerning the Anomeric Effect.The effect of substituent, degree of acetylation and positioning of the cationic charge on the antibacterial activity of quaternary chitosan derivativesTandem driven dynamic combinatorial resolution via Henry-iminolactone rearrangement.A late-stage intermediate in salinomycin biosynthesis is revealed by specific mutation in the biosynthetic gene cluster.Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis.YcaO domains use ATP to activate amide backbones during peptide cyclodehydrations.Consecutive carbon-carbon bond formation approach in tandem cyclization reactions.Mechanistic Studies on Covalent Assemblies of Metal-Mediated Hemi-Aminal Ethers.Anionic N-heterocyclic carbenes (NHCs): a versatile route to saturated NHCs bearing pendant weakly coordinating anions.One-step site-specific modification of native proteins with 2-pyridinecarboxyaldehydes.Triggering the directional selectivity of a ring-closure reaction leads to pyridoazacarbazoles with anticancer properties.Synthesis of cyclic 1,3-diols as scaffolds for spatially directed librariesOne-Step Synthetic Access to Isosteric and Potent Anticancer Nitrogen Heterocycles with the Benzo[c]phenanthridine Scaffold.Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversity.Metalated nitriles: S(N)i and S(N)i' installation of contiguous quaternary-tertiary and quaternary-quaternary centers.Low temperature n-butyllithium-induced [3,3]-sigmatropic rearrangement/electrophile trapping reactions of allyl-1,1-dichlorovinyl ethers. Synthesis of β-, γ- and δ-lactones.The biosynthesis of polyketide-derived polycyclic ethers.Synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascadesPolyketide biosynthesis in dinoflagellates: what makes it different?Synthetic endeavours towards oxasqualenoid natural products containing 2,5-disubstituted tetrahydrofurans--eurylene and teurilene.1,n-Hydrogen-atom transfer (HAT) reactions in which n≠5: an updated inventory.Catalytic Conia-ene and related reactions.The role of intramolecular self-destruction of reactive metabolic intermediates in determining toxicity.Alkaline earths as main group reagents in molecular catalysis.The Cation-π Interaction in Small-Molecule Catalysis.Development of a new air-stable structure-simplified nafuredin-γ analog as a potent and selective nematode complex I inhibitor.A ratiometric fluorescent probe for specific detection of cysteine over homocysteine and glutathione based on the drastic distinction in the kinetic profiles.Synthesis of anionic phosphorus-containing heterocycles by intramolecular cyclizations involving N-functionalized phosphinecarboxamides.Structure determination and total synthesis of (+)-16-hydroxy-16,22-dihydroapparicine.Ground-state dioxygen undergoes metal-free [3 + 2]-annulations with allenes and nitrosoarenes under ambient conditions.A dioxane template for highly selective epoxy alcohol cyclizations.1,4-Addition of bis(iodozincio)methane to α,β-unsaturated ketones: chemical and theoretical/computational studies.A radical access to highly functionalized tetrahydroxanthones.New reactions of N-tert-butylimines; formation of N-heterocycles by methyl radical elimination on flash vacuum thermolysis of N-benzylidene- and N-(2-pyridylmethylidene)-tert-butylamines.Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B.Diastereoselective intramolecular allyl transfer from allyl carbamate accompanied by 5-endo-trig ring closure.
P2860
Q26744255-0E3F95B2-4B32-4D18-AAB6-B253D285F11BQ27668138-31B9EBC2-0F7D-435E-B383-96E8C51AFDEBQ28266893-ED829F77-BF05-463D-9BAA-5966D32B8578Q30013723-E6ABAEEE-17BD-4D0B-A71F-0C8DE0D85A31Q30376131-06C6E2A9-DD36-4455-A37F-BFCCC5E2D9B6Q30848080-DE5A2627-9238-4750-B6E7-E22A020E4843Q33334544-F4CAC1A3-DDD9-4366-A646-575F8523A278Q34072847-AD98BAA0-8EB3-4015-9E47-7E59ABAE63EDQ34252286-EBB8FB2D-AC68-4826-A623-7AB78B857AD4Q34269958-943DEFF4-053B-453E-BDE5-9425B247E30FQ34587656-9F07A5EF-0F00-4E88-B71F-5BEFE93F9285Q34708596-B3FB937B-7FED-49ED-B30D-988A4F657139Q35242232-A3B7667C-BDEE-41D4-AD62-540D4F9522CDQ35590287-C8669D9A-3CA7-4018-A3E1-973ABC5AFD32Q35590719-2AEE7A63-424A-44E4-8C98-9D7928C01F81Q35992045-6929F128-3A83-407E-93F9-DB7941768CD2Q36010410-205D0EC1-1661-496E-9DF8-465D9B340D8BQ37227332-0CDC729B-D083-465F-BAE6-D35E858E8C89Q37306026-D4415340-B24F-46F2-8782-72606E2C6483Q37354546-80BBB72E-00CC-44E3-9C87-9AC264D180E1Q37379792-2D21CC4F-09D6-4D81-B510-5891A943EA6EQ37735711-D5DB92ED-75CF-4E07-8500-E2ACE4848345Q38220326-C51083EF-5FEC-47F8-BDC1-FD1F54563CF0Q38224576-B69C98C6-068C-43C2-A04B-64C91CC2E441Q38262807-5CAC90A5-5ADC-43A2-957D-80526284D1E9Q38510935-45270150-FABF-4FEB-A17E-F337A5E4677EQ38626757-A0F96E0F-3DF3-42FD-8390-EEDFEF83137CQ38707237-A3BA1249-FD13-45FB-B658-90AA0677CB9AQ38872688-8AC51B3F-EAF0-4945-94E7-3032E99F1F51Q39318747-B7370DE8-DCCA-4F19-B307-41CACCF7A040Q39556603-453C95F0-1993-4F25-B32A-51590B267FCDQ39840000-A2039144-AB6F-4D4E-A677-B1C2DC01A7ADQ41925286-86268430-91AD-4FC9-A956-90E4314438FFQ42039722-343ED9DD-8A5C-46CB-9920-9EF8FD9BE0FEQ42117738-C5FA7161-3586-4FD5-8298-6E3BDBEFE041Q42964863-0047667C-71B4-4A9A-9058-895AB2DC20C6Q43716897-11A492E5-CBB5-486A-9190-33E2448B8839Q43724235-6DC2BB9F-6590-41B9-ABDD-AE3A5AD143CCQ43730947-6720B7CD-B23C-4457-893D-425C1162773BQ43805306-F2DF360D-5075-4A30-827F-673E769EC0B4
P2860
description
1976 nî lūn-bûn
@nan
1976 թուականին հրատարակուած գիտական յօդուած
@hyw
1976 թվականին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Rules for ring closure
@ast
Rules for ring closure
@en
type
label
Rules for ring closure
@ast
Rules for ring closure
@en
prefLabel
Rules for ring closure
@ast
Rules for ring closure
@en
P3181
P356
P1476
Rules for ring closure
@en
P2093
Jack E. Baldwin
P3181
P356
10.1039/C39760000734
P577
1976-01-01T00:00:00Z