Výsledky vyhledávání - "Christoph Bihlmayer"

Reaction of 9-Borabicyclo[3.3.1]nonane with Alkyn-1-yltin Compounds. Molecular Structure of the 9-Propyn-1-yl-9-borabicyclo[3.3.1]nonane Pyridine Adduct

Autor: Khadija Shahid, Bernd Wrackmeyer, Christoph Bihlmayer, Wolfgang Milius

Publikováno v: Zeitschrift für Naturforschung B. 64:399-402

Trimethyl- and triethyl(propyn-1-yl)tin react with 9-borabicyclo[3.3.1.]nonane (9-BBN) mainly by exchange of the propynyl group against hydrogen, accompanied by numerous side reaction. This is in contrast to the findings for other alkynyltin compound

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6d1bc481c39b9c23dd5394397bf38ff1
https://doi.org/10.1515/znb-2009-0407

Zobrazit plný text záznamu

Organoborierung von Alkinylstannanen, XII. Alken‐ und Allen‐Synthesen unter Ausnutzung reaktiver Bor‐Kohlenstoff‐ und Bor‐Wasserstoff‐Bindungen

Autor: Christoph Bihlmayer, Bernd Wrackmeyer, Michael Schilling

Publikováno v: Chemische Berichte. 116:3182-3191

Die Spaltung der SnC-Bindung in Trialkylalkinylstannanen 2 mit Triethylboran (1a) verlauft uber eine Alkinylborat-Zwischenstufe A stereoselektiv zu Alken-Derivaten 3 mit Boryl- und Stannylgruppe in cis-Stellung. Die Reaktion dieser Alkene mit einem w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ed9714bda03b22ab67c314e4e87d3bad
https://doi.org/10.1002/cber.19831160916

Zobrazit plný text záznamu

Organoborierung von Alkinylstannanen, XI [1] Synthese von substituierten Alkenen ausgehend von 9-Borabicyclo [3.3.1] nonan-Derivaten / Organoboration of Alkynylstannanes, XI [1] Synthesis of Substituted Alkenes from 9-Borabicyclo[3,3,l]nonane Derivatives

Autor: Christoph Bihlmayer, Bernd Wrackmeyer

Publikováno v: Zeitschrift für Naturforschung B. 36:1265-1269

Organoboration, 9-Borabicyclo[3.3.1]nonanes, NMR Spectra New alkene derivatives are obtained from the reaction between 9-ethyl-borabicyclo-[3.3.1]nonane and alkynyl stannanes under kinetic or thermodynamic control. NMR evidence for a borate type inte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::382735dc570f7c9f508dfd15ea5d7e7e
https://doi.org/10.1515/znb-1981-1015

Zobrazit plný text záznamu

Reaction of 1,4-pentadiyne with diethylaminotrimethylstannane

Autor: Christoph Bihlmayer, Bernd Wrackmeyer

Publikováno v: Journal of Organometallic Chemistry. 266:33-36

The reaction between 1,4-pentadiyne and diethylaminotrimethylstannane leads predominantly to ( E )-2-diethylamino-4-trimethylstannyl-2,4-pentaenyne (with either a 1/1 or 1/2 mol ratio of 1,4-pentadiyne and diethylaminotrimethylstannane). With 1/2 sto

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fb8adef08ca97a82e5afa66cb3e02d03
https://doi.org/10.1016/0022-328x(84)80107-2

Zobrazit plný text záznamu

Organoboration of alkynlystannanes

Autor: Christoph Bihlmayer, Bernd Wrackmeyer, Sultan T. Abu-Orabi

Publikováno v: Journal of Organometallic Chemistry. 322:25-32

Tricyclic heterocycles ( 8 ) containing a stannacyclopentadiene unit are obtained as the major products (ρ 80%) from the reaction between diethynyldimethylstannane and B -alkyl-9-borabicyclo[3.3.1]nonanes ( 2 ). By comparison with the analogous reac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f4ad0e89f331f737d0258d175903f54b
https://doi.org/10.1016/0022-328x(87)85020-9

Zobrazit plný text záznamu

Organoborierung von Alkinylstannanen, XX [1] Oligomerisation von 1-Propinyltrimethylstannan / Organoboration of Alkynylstannanes, XX [1] Oligomerisation of 1-Propynyltrimethylstannane

Autor: Christoph Bihlmayer, Susanna Kerschl, Bernd Wrackmeyer

Publikováno v: Zeitschrift für Naturforschung B. 42:715-719

1-Propynylstannane (1) reacts with B-ethyl-9-borabicyclo[3.3.1]nonane (10) (ratio 2:1) to giva a new butadiene derivative (11). Attempts to oligomerize 1 by organoboration with trimethyl-borane (13) (ratio 2:1) lead to a hexatriene derivative (14). A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::441b2ab303917d7a77b9f339b75662b7
https://doi.org/10.1515/znb-1987-0613

Zobrazit plný text záznamu

ChemInform Abstract: UNEXPECTED PRODUCTS FROM THE REACTION OF ALKYNYLSTANNANES WITH 9-BORABICYCLO(3.3.1)NONANE

Autor: Bernd Wrackmeyer, Christoph Bihlmayer

Publikováno v: Chemischer Informationsdienst. 13

The reaction of 9-borabicyclo[3.3.1]nonane with alkynyltrimethylstannanes (Me3Sn–CC–R) yields a new alkene (R = But) and new allenes (R = Me3Si or Me3Sn); the formation of both types of compound is not consistent with hydroboration but involves e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::12b83ef95de417f7ce0982faa895da7d
https://doi.org/10.1002/chin.198212291

Zobrazit plný text záznamu

Unexpected products from the reaction of alkynylstannanes with 9-borabicyclo[3.3.1]nonane

Autor: Christoph Bihlmayer, Bernd Wrackmeyer

Publikováno v: Journal of the Chemical Society, Chemical Communications. :1093

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2482680f85a98da6e8139f509e22d461
https://doi.org/10.1039/c39810001093

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání