I agree that this site is using cookies. You can find further informations
here
.
X
Login
Merkliste (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
zur Desktop-Version
Toggle navigation
Merkliste
1 Ergebnisse
1
A Unified Approach to Polycyclic Alkaloids of the Ingenamin..:
Zhanchao Meng (4751931)
;
Simon M. Spohr (7313483)
;
Sandra Tobegen (11345891)
..
https://figshare.com/articles/journal_contribution/A_Unified_Approach_to_Polycyclic_Alkaloids_of_the_Ingenamine_Estate_Total_Syntheses_of_Keramaphidin_B_Ingenamine_and_Nominal_Njaoamine_I/16488233. , 2021
Link:
https://doi.org/10.1021/jacs.1c07955.s001
RT Journal T1
A Unified Approach to Polycyclic Alkaloids of the Ingenamine Estate: Total Syntheses of Keramaphidin B, Ingenamine, and Nominal Njaoamine I
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16488233&Exemplar=1&LAN=DE A1 Zhanchao Meng (4751931) A1 Simon M. Spohr (7313483) A1 Sandra Tobegen (11345891) A1 Christophe Farès (1958938) A1 Alois Fürstner (1610734) YR 2021 K1 Biophysics K1 Biochemistry K1 Evolutionary Biology K1 Ecology K1 Infectious Diseases K1 Chemical Sciences not elsewhere classified K1 suzuki coupling sequence K1 standard ruthenium catalysts K1 second lateral ring K1 lewis basic sites K1 flexibility opened opportunities K1 conspicuous tricyclic scaffold K1 bridgehead quarternary center K1 usually indiscriminative vis K1 allowed different handles K1 proved fully operative K1 arguably highest significance K1 ̀- vis K1 different π K1 unified approach K1 two consecutive K1 total syntheses K1 tertiary amines K1 synthesis ) K1 successfully interlinked K1 silanolate ligands K1 polycyclic alkaloids K1 particularly noteworthy K1 nominal njaoamine K1 membered cycle K1 macrocyclic rings K1 keramaphidin b K1 intricate hydroboration K1 equally rare K1 enveloping medium K1 common etheno K1 chosen targets K1 bridged diaza K1 biosynthesis pathway K1 best results JF https://figshare.com/articles/journal_contribution/A_Unified_Approach_to_Polycyclic_Alkaloids_of_the_Ingenamine_Estate_Total_Syntheses_of_Keramaphidin_B_Ingenamine_and_Nominal_Njaoamine_I/16488233 LK http://dx.doi.org/https://doi.org/10.1021/jacs.1c07955.s001 DO https://doi.org/10.1021/jacs.1c07955.s001 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)