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Chemistry – A European Journal, ISSN 0947-6539, 10/2015, Volume 21, Issue 44, pp. 15607 - 15621
Access to hydroxy‐functionalized P‐chiral phosphine–boranes has become an important field in the synthesis of P‐stereogenic compounds used as ligands in... 
boranes | phosphanes | reduction | stereospecificity | vibrationsl spectroscopy | DEPROTONATION | OP LIGANDS | PERFORMANCE | RESOLUTION | CATECHOLBORANE | HYDROFORMYLATIONS | CHEMISTRY, MULTIDISCIPLINARY | HETEROCYCLES | DEGRADATION | ASYMMETRIC HYDROGENATION | OXIDES
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2015, Volume 80, Issue 20, pp. 10025 - 10032
Phosphinylidene compounds R1R2P­(O)H are important functionalities in organophosphorus chemistry and display prototropic tautomerism. Quantifying the... 
PHOSPHINE-OXIDE | HYDROPHOSPHORYL COMPOUNDS | ACID | MECHANISM | CORRELATED MOLECULAR CALCULATIONS | AB-INITIO | CHEMISTRY, ORGANIC | DENSITY-FUNCTIONAL THEORY | GAUSSIAN-BASIS SETS | H-BOND | PHOSPHORUS-COMPOUNDS
Journal Article
2012, Research notes in mathematics, ISBN 9781466501928, Volume 11, ix, 163
"This book deals with the question on how NX(p), the number of solutions of mod p congruences, varies with p when the family (X) of polynomial equations is... 
Polynomials | Cohomology operations | Number theory | Representations of groups
Book
Transplantation, ISSN 0041-1337, 11/2019, Volume 103, pp. S104 - S105
Journal Article
European Journal of Inorganic Chemistry, ISSN 1434-1948, 03/2019, Volume 2019, Issue 11, pp. 1621 - 1632
Herein we report on the synthesis of a set of transient N-(P-III)-phosphanyl and N-(P-V)-phosphoroselenoyl acyclic diaminocarbenes by deprotonation of the... 
Phosphanes | Cyclization | Nitrogen heterocycles | Azomethine ylides | Carbenes | 1,2-MIGRATION | SALTS | PRECURSORS | IMIDAZOL-2-YLIDENES | CHEMISTRY, INORGANIC & NUCLEAR | or physical chemistry | Analytical chemistry | Polymers | Material chemistry | Chemical Sciences | Theoretical and
Journal Article
by Aaboud, M and Aad, G and Abbott, B and Abdallah, J and Abdinov, O and Abeloos, B and Abidi, S H and AbouZeid, O S and Abraham, N L and Abramowicz, H and Abreu, H and Abreu, R and Abulaiti, Y and Acharya, B S and Adachi, S and Adamczyk, L and Adelman, J and Adersberger, M and Adye, T and Affolder, A A and Agatonovic-Jovin, T and Agheorghiesei, C and Aguilar-Saavedra, J A and Ahlen, S P and Ahmadov, F and Aielli, G and Akatsuka, S and Akerstedt, H and Åkesson, T P. A and Akimov, A V and Alberghi, G L and Albert, J and Albicocco, P and Verzini, M J. Alconada and Aleksa, M and Aleksandrov, I N and Alexa, C and Alexander, G and Alexopoulos, T and Alhroob, M and Ali, B and Aliev, M and Alimonti, G and Alison, J and Alkire, S P and Allbrooke, B M. M and Allen, B W and Allport, P P and Aloisio, A and Alonso, A and Alonso, F and Alpigiani, C and Alshehri, A A and Alstaty, M and Gonzalez, B Alvarez and Piqueras, D Álvarez and Alviggi, M G and Amadio, B T and Coutinho, Y Amaral and Amelung, C and Amidei, D and Santos, S P. Amor Dos and Amorim, A and Amoroso, S and Amundsen, G and Anastopoulos, C and Ancu, L S and Andari, N and Andeen, T and Anders, C F and Anders, J K and Anderson, K J and Andreazza, A and Andrei, V and Angelidakis, S and Angelozzi, I and Angerami, A and Anisenkov, A V and Anjos, N and Annovi, A and Antel, C and Antonelli, M and Antonov, A and Antrim, D J and Anulli, F and Aoki, M and Bella, L Aperio and Arabidze, G and Arai, Y and Araque, J P and Ferraz, V Araujo and Arce, A T. H and Ardell, R E and Arduh, F A and Arguin, J-F and Argyropoulos, S and Arik, M and Armbruster, A J and Armitage, L J and Arnaez, O and ... and ATLAS Collaboration and Brookhaven National Lab. (BNL), Upton, NY (United States) and Oak Ridge National Laboratory, Oak Ridge Leadership Computing Facility (OLCF) and eSSENCE: The e-Science Collaboration and Lund University and Partikelfysik and Lunds universitet and Particle Physics
The European Physical Journal C, ISSN 1434-6044, 6/2017, Volume 77, Issue 6, pp. 1 - 40
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2015, Volume 2015, Issue 2, pp. 302 - 308
A robust solid‐phase synthesis was developed to obtain original oligonucleotides (ONs) functionalized at their 5′ end with modified triphosphate (TP) moieties,... 
Phosphorylation | Triphosphates | RNA | Thiotriphosphates | Solid‐phase synthesis | Oligonucleotides | Solid-phase synthesis | TRIPHOSPHATE ANALOGS | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | NUCLEOTIDES | MESSENGER-RNA | BACILLUS-SUBTILIS | NUCLEOSIDE 5'-TRIPHOSPHATES | DEGRADATION
Journal Article