Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Robert E. Kinder"'
Publikováno v:
Journal of the American Chemical Society. 128:9066-9073
Reaction of benzyl (2,2-diphenyl-4,5-hexadienyl)carbamate (4) with a catalytic 1:1 mixture of Au[P(t-Bu)2(o-biphenyl)]Cl (2) and AgOTf (5 mol %) in dioxane at 25 degrees C for 45 min led to isolation of benzyl 4,4-diphenyl-2-vinylpyrrolidine-1-carbox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00efa6e57fb38cdaad087e016469d2a9
https://doi.org/10.1021/ja062045r
https://doi.org/10.1021/ja062045r
Publikováno v:
ChemInform. 39
Reaction of 2,3-pentadienyl benzoate with benzyl carbamate catalyzed by a 1:1 mixture of (NHC)AuCl and AgOTf in dioxane at 23 °C for 5 h led to isolation of (E)-4-(benzyloxycarbonylamino)-2-pentenyl benzoate in 84% yield as a single regio- and diast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20243ba2917fc55bcc450743ef2f3426
https://doi.org/10.1002/chin.200848052
https://doi.org/10.1002/chin.200848052
Autor:
Robert E. Kinder, Ross A. Widenhoefer
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[6163-58-2] C21H21P (MW 304.37) InChI = 1S/C21H21P/c1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3/h4-15H,1-3H3 InChIKey = COIOYMYWGDAQPM-UHFFFAOYSA-N (reagent used as a ligand in transition metal catalyzed reactions) Physical Data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d7ce6dbde544fdb7e355c2e57c99da5
https://doi.org/10.1002/047084289x.rn00909
https://doi.org/10.1002/047084289x.rn00909
Reaction of 2,3-pentadienyl benzoate with benzyl carbamate catalyzed by a 1:1 mixture of (NHC)AuCl and AgOTf in dioxane at 23 degrees C for 5 h led to isolation of (E)-4-(benzyloxycarbonylamino)-2-pentenyl benzoate in 84% yield as a single regio- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d375518d7abbca54993fd5a509ec1f
https://europepmc.org/articles/PMC2727634/
https://europepmc.org/articles/PMC2727634/
Autor:
Ross A. Widenhoefer, Robert E. Kinder
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[130296-28-5] C16H24F6RhSb (MW 555.02) InChI = 1S/2C8H12.6FH.Rh.Sb/c2*1-2-4-6-8-7-5-3-1;;;;;;;;/h2*1-2,7-8H,3-6H2;6*1H;;/q;;;;;;;;+1;+5/p-6/b2*2-1-,8-7-;;;;;;;; InChIKey = BROZUPPJWNODCU-SXGOCSEPSA-H (catalyst precursor for enantioselective hydrogena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23a8f1d94be849d32b7c07aebdaa77b1
https://doi.org/10.1002/047084289x.rn00893
https://doi.org/10.1002/047084289x.rn00893
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a535e9c05a8180bb612c803576e7545
https://doi.org/10.1002/chin.200648036
https://doi.org/10.1002/chin.200648036
Autor:
Robert E. Kinder, Ross A. Widenhoefer
Publikováno v:
ChemInform. 37
[reaction: see text] Reaction of enyne 1 with catecholborane catalyzed by a 1:1 mixture of [Rh(COD)(2)](+)SbF(6)(-) and (S)-BINAP (5 mol %) followed by Pd-catalyzed arylation with p-IC(6)H(4)CF(3) gave benzylidenecyclopentane 5 in 65% yield with 88%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64dcecbfae4fed30203dfeeada367662
https://doi.org/10.1002/chin.200637033
https://doi.org/10.1002/chin.200637033
Autor:
Ross A. Widenhoefer, Robert E. Kinder
Publikováno v:
Synfacts. 2006:0708-0708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eb3e35c2ae4e2e67c8838d6f771b3bc
https://doi.org/10.1055/s-2006-941856
https://doi.org/10.1055/s-2006-941856
Publikováno v:
Organic Letters; May2008, Vol. 10 Issue 14, p3157-3159, 3p
Autor:
James C. Taylor
This monograph includes five chapters that detail recent advancements in chemistry research. Chapter One describes the presence of micropollutants that disrupt the endocrine system in drinking water and discusses challenges and strategies of removing