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Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[80-11-5] C8H10N2O3S (MW 214.27) InChI = 1S/C8H10N2O3S/c1-7-3-5-8(6-4-7)14(12,13)10(2)9-11/h3-6H,1-2H3 InChIKey = FFKZOUIEAHOBHW-UHFFFAOYSA-N (precursor of diazomethane1a) Alternate Names: Diazald; p-tolylsulfonylmethylnitrosamide. Physical Data: mp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddb748e84c651ae4790217d6ad1b1131
https://doi.org/10.1002/047084289x.rm221.pub2
https://doi.org/10.1002/047084289x.rm221.pub2
Autor:
John I. Trujillo
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[89979-13-5] C8H8ClNO4S (MW 249.665) InChI = 1S/C8H8ClNO4S/c9-15(12,13)10-8(11)14-6-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11) InChIKey = BCSYQDOKTDVISP-UHFFFAOYSA-N (sulfamidating reagent; precursor for modified Burgess reagents) Alternate Names: benzyl N-ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9058bc5916f3f864ce6a3f996349880
https://doi.org/10.1002/047084289x.rn01979
https://doi.org/10.1002/047084289x.rn01979
Autor:
Merritt B. Andrus
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[165275-73-0] C17H30CuF12N2O2Sb2 (MW 829.48) InChI = 1S/C17H30N2O2.Cu.12FH.2Sb/c1-15(2,3)11-9-20-13(18-11)17(7,8)14-19-12(10-21-14)16(4,5)6;;;;;;;;;;;;;;;/h11-12H,9-10H2,1-8H3;;12*1H;;/q;+2;;;;;;;;;;;;;2*+5/p-12/t11-,12-;;;;;;;;;;;;;;;/m1 /s1 InChIKe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b1d40eb5d99986395d3e029649f96e
https://doi.org/10.1002/047084289x.rn01729
https://doi.org/10.1002/047084289x.rn01729
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[6655-31-8] C6H4N4O4S (MW 228.21) InChI = 1S/C6H4N4O4S/c7-8-9-15(13,14)6-4-2-1-3-5(6)10(11)12/h1-4H InChIKey = MNMURNLWLUKMSZ-UHFFFAOYSA-N (1,3-dipolar reagent that undergoes cycloaddition to alkenes, enamines, enol ethers, and enynes1) Physical Data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b704fdf53ff4e33bdd57ab9c77304a3
https://doi.org/10.1002/047084289x.rn026.pub2
https://doi.org/10.1002/047084289x.rn026.pub2
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
C34H36P2 (MW 505.8) InChI = 1S/C34H36P2/c1-5-15-27(16-6-1)35(28-17-7-2-8-18-28)33-25-13-23-31(33)32-24-14-26-34(32)36(29-19-9-3-10-20-29)30-21-11-4-12-22-30/h1-12,15-22,31-34H,13-14,23-26H2/t31-,32-,33-,34-/m1/s1 InChIKey = UKCDADXCAXXBGR-YFRBGRBWSA-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::023bf81abf0c23d832ed314793293649
https://doi.org/10.1002/047084289x.rn00187.pub2
https://doi.org/10.1002/047084289x.rn00187.pub2
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[14542-93-9] C9H17N (MW 139.26) InChI = 1S/C9H17N/c1-8(2,3)7-9(4,5)10-6/h7H2,1-5H3 InChIKey = YVPXQMYCTGCWBE-UHFFFAOYSA-N (adds organometallic reagents to give α-metalloaldimines; synthetically useful acyl anion equivalent4) Alternate Name: isooctyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82ce34e30a8c4610b27dce7300fc6f44
https://doi.org/10.1002/047084289x.rt061.pub2
https://doi.org/10.1002/047084289x.rt061.pub2
Autor:
Takayuki Kato
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[1269247-13-3] C7H11NO2S (MW 173.05) InChI = 1S/C7H11NO2S/c1-2-5-11-8-6(9)3-4-7(8)10/h2-5H2,1H3 InChIKey = STDGTTXRFKALAY-UHFFFAOYSA-N (reagent for the allylic functionalization of aryl cycloalkenes and asymmetric oxysulfenylation of alkenes) Alterna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7bea14aa5ed99e7c07c0451e89a884f
https://doi.org/10.1002/047084289x.rn01687
https://doi.org/10.1002/047084289x.rn01687
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
(1,1,2,2-Tetrafluoroethyl-N,N-dimethylamine) [1550-50-1] C4H7F4N (MW 145.1) InChI = 1S/C4H7F4N/c1-9(2)4(7,8)3(5)6/h3H,1-2H3 InChIKey = VIRGYRZBWQFJGJ-UHFFFAOYSA-N (conversion of alcohols to alkyl fluorides,1 carboxylic acids to acyl fluorides,1 activ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c326759f31a439c8d853de75679942fb
https://doi.org/10.1002/047084289x.rn01690
https://doi.org/10.1002/047084289x.rn01690
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[3383-21-9] C14H20O2 (MW 220.31) InChI = 1S/C14H20O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8H,1-6H3 InChIKey = NOUZOVBGCDDMSX-UHFFFAOYSA-N (reacts with primary amines to give different products depending on the alkyl substituent: benzoxazoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71898e082f64ff7765de98c0e440c26d
https://doi.org/10.1002/047084289x.rd057.pub2
https://doi.org/10.1002/047084289x.rd057.pub2
Autor:
Rajender Salla
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
Racemate [6002-45-5] InChI = 1S/C10H15OPS/c1-10(2,3)12(11,13)9-7-5-4-6-8-9/h4-8H,1-3H3,(H,11,13) InChIKey = ACQNBIJCKLUKMY-UHFFFAOYSA-N (S)-Enantiomer [55705-77-6] InChI = 1S/C10H15OPS/c1-10(2,3)12(11,13)9-7-5-4-6-8-9/h4-8H,1-3H3,(H,11,13)/t12-/m1/s1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec80ddd8241b053f7dba534060930874
https://doi.org/10.1002/047084289x.rn01592
https://doi.org/10.1002/047084289x.rn01592