C. Sahlberg

发表

Aliskiren displays long-lasting interactions with human renin

L. Vrang, Ian R. Henderson, U. Danielson, 2012, Naunyn-Schmiedeberg's Archives of Pharmacology.

C. Sund, K. Jansson, C. Sahlberg, 2004 .

Allenes and Acetylenes. XVIII. Synthesis of 3-Pyrrolines by Silver(I)-catalyzed Cyclization of Allenic Amines.

K. Lempert, J. Møller, K. Luthman, 1979 .

Discovery and Optimization of a Compound Series Active against Trypanosoma cruzi, the Causative Agent of Chagas Disease.

Ana Rodriguez, L. Stojanovski, K. Read, 2020, Journal of medicinal chemistry.

Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs.

L. Vrang, B. Oberg, J. Morin, 1996, Journal of medicinal chemistry.

Synthesis of tritium labelled DSP 4, a selective noradrenaline neurotoxin

L. Gawell, C. Sahlberg, 1985 .

Allenes and Acetylenes. XXIV. Synthesis of alpha-Allenic Amines by Organocuprate Reactions of Acetylenic Aminoethers.

T. Högberg, L. Johansson, M. Persson, 1982 .

Aliskiren displays long-lasting interactions with human renin

L. Vrang, E. Lindström, Ian R. Henderson, 2012, Naunyn-Schmiedeberg's Archives of Pharmacology.

SYNTHESIS OF CONJUGATED DIENES BY NICKEL‐CATALYZED REACTIONS OF 1,3‐ALKADIEN‐2‐YL PHOSPHATES WITH GRIGNARD REAGENTS

A. Quader, A. Claesson, C. Sahlberg, 1984 .

Antibacterial Isoquinoline Alkaloids from the Fungus Penicillium Spathulatum Em19

B. Guss, B. Öberg, Joakim Bjerketorp, 2019, Molecules.

Synthesis and anti-HIV activities of urea-PETT analogs belonging to a new class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors.

L. Vrang, L Vrang, M Högberg, 1998, Bioorganic & medicinal chemistry letters.

Mechanistic aspects of reductions of allylic ethers and acetates with organocuprates

A. Claesson, C. Sahlberg, 1979 .

Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant.

S. Sigurdsson, T. Unge, Hong Zhang, 2002, European journal of biochemistry.

Allenes and acetylenes. 28. On the mechanism of reduction of propargylic ethers and acetates with organocuprates

A. Claesson, C. Sahlberg, 1984 .

Allenes and acetylens—XXIII1

A. Claesson, C. Sahlberg, 1982 .

Synthesis and monoamine oxidase inhibitory activities of alpha-allenic amines in vivo and in vitro. Different activities of two enantiomeric allenes.

S. Ross, I. Fagervall, A. Claesson, 1983, Journal of medicinal chemistry.

Reductions of allylic compounds with organocuprates

A. Claesson, C. Sahlberg, 1979 .

Design and synthesis of potent macrocyclic renin inhibitors.

N. Borkakoti, Elizabeth Hamelink, L. Vrang, 2011, Bioorganic & medicinal chemistry letters.

ALLENES AND ACETYLENES. XXIII. SYNTHESIS OF α‐ALLENIC AMINES VIA ALLENIC IMINES OBTAINED FROM ORGANOCOPPER REACTIONS

A. Claesson, C. Sahlberg, 1982 .

Synthesis of carbon‐14 labelled ropivacaine, a local anaesthetic agent

C. Sahlberg, 1987 .

Synthesis of 3′-ethynylthymidine, 3′-vinylthymidine and 3′-bromovinylthymidine as potential antiviral agents

C. Sahlberg, 1992 .

Synthesis of 3′‐Ethynylthymidine, 3′‐Vinylthymidine, and 3′‐ Bromovinylthymidine as Potential Antiviral Agents.

C. Sahlberg, 1992 .

Inhibition of human immunodeficiency virus type 1 wild-type and mutant reverse transcriptases by the phenyl ethyl thiazolyl thiourea derivatives trovirdine and MSC-127.

L. Vrang, B. Oberg, T. Unge, 1995, Antiviral research.

Synthesis of a Tritiated LPS Inhibitor Derived from 3-Deoxy-D-manno-2-octulosonic Acid (KDO). A Cautionary Note Regarding Amide Synthesis from Azides via Phosphine Imines.

A. Jansson, A. Claesson, C. Sahlberg, 1989 .

Synthesis of [14C]amiflamine ‐ an MAO‐A inhibitor

L. Gawell, C. Sahlberg, 1987 .

Allenes and acetylenes XXVI. Organocuprate reactions of 1,3-alkadien-2-yl phosphates. a new approach to the synthesis of allenes

A. Quader, A. Claesson, C. Sahlberg, 1983 .

Labradorins with Antibacterial Activity Produced by Pseudomonas sp.

Joakim Bjerketorp, A. Broberg, J. Levenfors, 2017, Molecules.

Antibacterial 3,6-Disubstituted 4-Hydroxy-5,6-dihydro-2H-pyran-2-ones from Serratia plymuthica MF371-2.

B. Guss, B. Öberg, Joakim Bjerketorp, 2017, Journal of natural products.

Backbone nuclear magnetic resonance assignment of human deoxyuridine 5′-triphosphate nucleotidohydrolase (dUTPase)

J. Isaksson, Esmeralda A. Woestenenk, T. Agback, 2013, Biomolecular NMR Assignments.

Backbone nuclear magnetic resonance assignment of human deoxyuridine 5′-triphosphate nucleotidohydrolase (dUTPase)

Esmeralda A. Woestenenk, T. Agback, C. Sahlberg, 2013, Biomolecular NMR Assignments.

Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues.

L. Vrang, B. Oberg, T. Unge, 1999, Journal of medicinal chemistry.

Synthesis of tritium labelled (−)-3-PPP, a selective dopamine autoreceptor agonist

S. Thorberg, L. Gawell, L. Johansson, 1986 .

Development of Non-Nucleoside Reverse Transcriptase Inhibitors for Anti- HIV Therapy

C. Sahlberg, Xiao-Xiong Zhou, 2008 .

The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase

L. Vrang, T. Unge, J. Deeter, 1995, Antimicrobial agents and chemotherapy.

Allenes and acetylenes XVII. Allenic amines from organocuprate reactions

A. Claesson, C. Sahlberg, 1978 .