Výsledky vyhledávání

A Direct Organocatalytic Enantioselective Route to Functionalized trans-Diels–Alder Products Having the Norcarane Scaffold

Autor: Karl Anker Jørgensen, Niklas Lawaetz Østergaard, Casper L. Barløse, Marc V. Iversen, René Slot Bitsch

Publikováno v: Barløse, C L, Østergaard, N L, Bitsch, R S, Iversen, M V & Jørgensen, K A 2021, ' A Direct Organocatalytic Enantioselective Route to Functionalized trans-Diels–Alder Products Having the Norcarane Scaffold ', Angewandte Chemie-International Edition, vol. 60, no. 33, pp. 18318-18327 . https://doi.org/10.1002/anie.202106598

An enantioselective methodology to construct trans-Diels–Alder scaffolds by organocatalysis with excellent selectivity, high yield and up to five contiguous stereocenters is presented. The reaction concept integrates the halogen effect and a novel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29fdc3be3533e8567a966bd29946c4f2
https://pure.au.dk/portal/da/publications/a-direct-organocatalytic-enantioselective-route-to-functionalized-transdielsalder-products-having-the-norcarane-scaffold(1e357129-a6fc-44ca-b833-2be270153bb2).html

Zobrazit plný text záznamu

Insights into the electronic structure and mechanism of norcarane hydroxylation by OxoMn(V) porphyrin complexes: A density functional theory study

Autor: Zhifeng Ma, Naoki Nakatani, Masahiko Hada

Publikováno v: Journal of computational chemistryREFERENCES. 42(27)

Norcarane hydroxylation by neutral [PorMn(V)O-L] (L═OH- , F- ) and cationic [PorMn(V)O-L]+ (L═H2 O, imidazole) oxoMn(V) porphyrin complex models has been investigated by density functional theory calculations to better understand the reaction mec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc91c62e6e46455769b7550949bafe7
https://pubmed.ncbi.nlm.nih.gov/34448235

Zobrazit plný text záznamu

Synthetic Methods for the Preparation of Norcarane Scaffolds. A Review

Autor: Andrés López Radcenco, Guillermo Moyna, Florencia Parpal, Macarena Eugui

Publikováno v: Organic Preparations and Procedures International. 50:260-287

The bicyclo[4.1.0]heptane, or norcarane, fused ring system is present in a vast number of natural products, including the conifer sesquiterpenes thujopsene and hinokiic acid,1 the marasmanes isovel...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ee5c53887eac4834ec3278ba8d2a34d4
https://doi.org/10.1080/00304948.2018.1462048

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Profiling Mechanisms of Alkane Hydroxylase Activity In Vivo Using the Diagnostic Substrate Norcarane

Autor: Rozhkova-Novosad, Elena A., Chae, Jong-Chan, Zylstra, Gerben J., Bertrand, Erin M., Alexander-Ozinskas, Marselle, Deng, Dayi, Moe, Luke A., van Beilen, Jan B., Danahy, Michael, Groves, John T., Austin, Rachel N.

Publikováno v: In Chemistry & Biology 2007 14(2):165-172

Zobrazit plný text záznamu

Use of cycloaddition reactions and photochemical transformations in the preparation of norcarane derivatives

Autor: Andrés López Radcenco, Guillermo Moyna, Carlos Tabarez

Publikováno v: Tetrahedron Letters. 57:1515-1517

We detail a strategy for the preparation of bicyclo[4.1.0]heptanes, or norcaranes, based on Diels–Alder reactions and photochemical transformations. As the latter step of the process proceeds with unique regio and stereochemistries, the regio and s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4f8d4611e564ee86015b4b3010145073
https://doi.org/10.1016/j.tetlet.2016.02.087

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání