Zobrazeno 1 - 10
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pro vyhledávání: ''
Autor:
Daniela Sustac Roman
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[372-64-5] (C2F6S2) (MW 202.14) InChI = 1S/C2F6S2/c3-1(4,5)9-10-2(6,7)8 InChIKey = CGMFFOXAQVRUAZ-UHFFFAOYSA-N (source of radical SCF3 for preparation of trifluoromethyl sulfides) Alternate Names: trifluoromethyldisulfide, hexafluorodimethyldisulfide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::330e73a98bf4405dc03fc1b97f79d0fd
https://doi.org/10.1002/047084289x.rn01735
https://doi.org/10.1002/047084289x.rn01735
Autor:
D. Fray
Publikováno v:
Molten Salts Chemistry and Technology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d78dd93200b97ca5a0076ae9eeee6570
https://doi.org/10.1002/9781118448847.ch1b
https://doi.org/10.1002/9781118448847.ch1b
Autor:
James J. Mousseau
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[627-11-2] C3H4Cl2O2 (MW 142.97) InChI = 1S/C3H4Cl2O2/c4-1-2-7-3(5)6/h1-2H2 InChIKey = SVDDJQGVOFZBNX-UHFFFAOYSA-N (reagent used as a bis-electrophile, commonly used in the preparation of oxazolidinones) Alternate Names: 2-chloroethyl chloroformate;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b706f39d34f823a88a5a5ed2181c0f3c
https://doi.org/10.1002/047084289x.rn01309
https://doi.org/10.1002/047084289x.rn01309
Autor:
Craig R. Smith
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[17865-20-2] C9H15SiCl (MW 186.76) InChI = 1S/C9H15ClSi/c1-4-7-11(10,8-5-2)9-6-3/h4-6H,1-3,7-9H2 InChIKey = LMQNPINUXNVGGV-UHFFFAOYSA-N (dendrimer capping agent) Alternate Names: triallylchlorosilane, triallylsilyl chloride. Physical Data: bp 97–98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f856a7ad9594755e6098e6ca6fde6aff
https://doi.org/10.1002/047084289x.rn01223
https://doi.org/10.1002/047084289x.rn01223
Autor:
Jürgen Schatz, Gerhard Maas
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[134436-16-1] C9H18ClF3O3SSi (MW 326.83) InChI = 1S/C9H18ClF3O3SSi/c1-7(2,3)18(10,8(4,5)6)16-17(14,15)9(11,12)13/h1-6H3 InChIKey = KFJSFTNXTRLUFF-UHFFFAOYSA-N (reagent used for the preparation of unsymmetrically substituted silaketals tert-Bu2Si(OR1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cddc1c262ec1cb8a275a12738e6c66a
https://doi.org/10.1002/047084289x.rn00436
https://doi.org/10.1002/047084289x.rn00436
Autor:
Serge L. Beaucage
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[89992-70] C9H18ClN2OP (MW 236.68) InChI = 1S/C9H18ClN2OP/c1-8(2)12(9(3)4)14(10)13-7-5-6-11/h8-9H,5,7H2,1-4H3 InChIKey = QWTBDIBOOIAZEF-UHFFFAOYSA-N (reagent widely used for the phosphinylation of the 3′-hydroxy function of modified and unmodified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::217ea4e461cc07c3b162ce9e89742d6c
https://doi.org/10.1002/047084289x.rn00060
https://doi.org/10.1002/047084289x.rn00060
Autor:
Yeun‐Min Tsai
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[98486-13-6] C6H11ClO (MW 134.61) InChI = 1S/C6H11ClO/c1-2-3-4-5-8-6-7/h2H,1,3-6H2 InChIKey = JZTPLKRKISEKTC-UHFFFAOYSA-N (protection of alcohols1) Alternate Name: 4-pentenyloxymethyl chloride; POMCl. Physical Data: bp 158–160 °C/760 mmHg, 34–38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::315157671047e83118364ca60f8955b4
https://doi.org/10.1002/047084289x.rc121
https://doi.org/10.1002/047084289x.rc121
Autor:
Peter G. M. Wuts
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[88023-78-3] C9H11ClO2 (MW 186.65) InChI = 1S/C9H11ClO2/c1-11-9-4-2-8(3-5-9)6-12-7-10/h2-5H,6-7H2,1H3 InChIKey = DNZXMWKFPMIKRG-UHFFFAOYSA-N (protection of alcohols;1 one-carbon synthon4) Alternate Names: PMBM-Cl; 4-methoxybenzyl chloromethyl ether.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec7bd1877c25f23939c1190435d1b7d8
https://doi.org/10.1002/047084289x.rm083
https://doi.org/10.1002/047084289x.rm083
Autor:
Larry C. Blaszczak
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[77425-85-5] C16H38SiSn (MW 377.34) InChI = 1S/C4H11Si.3C4H9.Sn/c1-5(2,3)4;3*1-3-4-2;/h1H2,2-4H3;3*1,3-4H2,2H3; InChIKey = IOKUELHTFOPLKK-UHFFFAOYSA-N (precursor to trimethylsilylmethyllithium; methylenation of aldehydes and ketones) Alternate Name:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9874b11327b1ef8ec6ce058b2a304cbe
https://doi.org/10.1002/047084289x.rt185
https://doi.org/10.1002/047084289x.rt185
Autor:
Alan Armstrong
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[16421-86-6] C12H8O5P2 (MW 294.14) InChI = 1S/C12H8O5P2/c1-2-6-10-9(5-1)13-18(14-10)17-19-15-11-7-3-4-8-12(11)16-19/h1-8H InChIKey = DNHMXPCFVZGYMO-UHFFFAOYSA-N (reagent for peptide synthesis1) Physical Data: mp 72 °C; bp 156 °C/0.25 mmHg; n20D 1.5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a012f921d1f98d48a8786f71ebf56e0d
https://doi.org/10.1002/047084289x.rb182
https://doi.org/10.1002/047084289x.rb182