about
Synthesis and biological evaluation of epidithio-, epitetrathio-, and bis-(methylthio)diketopiperazines: synthetic methodology, enantioselective total synthesis of epicoccin G, 8,8'-epi-ent-rostratin B, gliotoxin, gliotoxin G, emethallicin E, and haSynthesis and antiproliferative properties of a new ceramide analog of varacin.Synthesis of Diiron(I) Dithiolato Carbonyl ComplexesThe chemistry behind redox regulation with a focus on sulphur redox systems.Chemical foundations of hydrogen sulfide biology.Recent approaches for the direct use of elemental sulfur in the synthesis and processing of advanced materials.Polysulfide-1-oxides react with peroxyl radicals as quickly as hindered phenolic antioxidants and do so by a surprising concerted homolytic substitution.Synthesis and redox-enzyme modulation by amino-1,4-dihydro-benzo[d][1,2]dithiine derivatives.Influence of methanethiol on biological sulphide oxidation in gas treatment system.Experimental investigations and ab initio studies of selenium(II) dialkanethiolates, Se(SR)2.A one-pot synthesis of polysulfane-bearing block copolymer nanoparticles with tunable size and refractive index.Chemical Biology of H2S Signaling through Persulfidation.Preparation of hyperstar polymers with encapsulated Au25(SR)18 clusters as recyclable catalysts for nitrophenol reduction.Synthesis of Thioethers and Thioesters with Alkyl Arylsulfinates as the Sulfenylation Agent under Metal-Free Conditions.Organotrisulfide: A High Capacity Cathode Material for Rechargeable Lithium Batteries.Sulfoxylic and Thiosulfurous Acids and their Dialkoxy Derivatives7 Oxygen, sulfur, selenium and telluriumA prototype hybrid 7π quinone-fused 1,3,2-dithiazolyl radical
P2860
Q36376066-24852F0D-FD59-4934-9045-C6211C27A7C8Q36479447-94DA00AB-FE02-4B92-ABFF-94234044E18AQ37067812-8F5DEFCD-120F-4290-84D6-734018D86D7CQ37111950-24294E9E-B801-4F69-B1FA-C284CEB6841FQ38121347-D741E7A1-8EE9-4041-B5F1-E877701E1BA4Q38316178-A2CE8F9E-2A04-4AC1-B21A-0D5B2278F1B9Q38676404-8330CFF3-4A67-4BC1-BD1F-681F13A20DBFQ41440421-947269CD-E64D-42D0-9F1B-82EA1E7736F4Q43342317-9544F142-DFE3-4AB1-A1D8-7644894055A5Q45128361-D4A7FF7E-B298-498D-BA0F-12921EC46A09Q47341600-84386280-9897-441C-B635-C45D473C1C1DQ47430972-3D55F3C6-97E0-419C-B7F9-5066C22B889DQ48181088-D4CF4A5C-2F03-4286-9834-C58F3088FA26Q50214814-49204530-D567-459D-8799-DF896E55F710Q51250990-DA225BFA-D5F9-48E7-ADB0-C1110EF2E941Q57379146-59FB7FC1-60DB-46A0-A6BB-63D5C0FB9699Q57565498-673835B6-A10A-4D57-92FD-B393B0AF8FF5Q57878492-60D44EAB-815B-44F1-840D-E8405BEAABD5
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The chemistry of organic polysulfanes R-S
@nl
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@ast
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@en
type
label
The chemistry of organic polysulfanes R-S
@nl
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@ast
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@en
prefLabel
The chemistry of organic polysulfanes R-S
@nl
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@ast
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@en
P356
P1433
P1476
The chemistry of organic polysulfanes R-S(n)-R (n > 2).
@en
P2093
Ralf Steudel
P304
P356
10.1021/CR010127M
P577
2002-11-01T00:00:00Z