[图书][B] Biocatalysis in the pharmaceutical and biotechnology industries

RN Patel - 2006 - taylorfrancis.com
Because enzyme-catalyzed reactions exhibit higher enantioselectivity, regioselectivity,
substrate specificity, and stability, they require mild conditions to react while prompting …

Syntheses of 4'-C-Ethynyl-β-d-arabino- and 4'-C-Ethynyl-2'-deoxy-β-d-ribo-pentofuranosylpyrimidines and -purines and Evaluation of Their Anti-HIV Activity

H Ohrui, S Kohgo, K Kitano, S Sakata… - Journal of medicinal …, 2000 - ACS Publications
4 '-C-Ethynyl-β-d-arabino-and 4 '-C-ethynyl-2 '-deoxy-β-d-ribo-pentofuranosylpyrimidine and-
purine nucleosides were synthesized and evaluated for their in vitro anti-HIV activity. The …

Nucleosides and Nucleotides. 175. Structural Requirements of the Sugar Moiety for the Antitumor Activities of New Nucleoside Antimetabolites, 1-(3-C-Ethynyl-β-dr ibo …

H Hattori, E Nozawa, T Iino, Y Yoshimura… - Journal of medicinal …, 1998 - ACS Publications
We previously designed 1-(3-C-ethynyl-β-d-ribo-pentofuranosyl) uracil (EUrd) and its
cytosine congener (ECyd) as potential multifunctional antitumor nucleoside antimetabolites …

Stereocontrolled syntheses of deoxyribonucleosides via photoinduced electron-transfer deoxygenation of benzoyl-protected ribo-and arabinonucleosides

Z Wang, DR Prudhomme, JR Buck… - The Journal of …, 2000 - ACS Publications
The stereocontrolled, de novo syntheses of β-2 '-deoxy-, α-2 '-deoxy-, β-3 '-deoxy-, and β-2 ',
3 '-dideoxyribonucleosides are described. Strategically protected ribose, arabinose, and …

Ligand Design and Preparation, Photophysical Properties, and Device Performance of an Encapsulated-Type Pseudo-Tris(heteroleptic) Iridium(III) Emitter

V Adamovich, L Benavent, PLT Boudreault… - Inorganic …, 2023 - ACS Publications
The organic molecule 2-(1-phenyl-1-(pyridin-2-yl) ethyl)-6-(3-(1-phenyl-1-(pyridin-2-yl) ethyl)
phenyl) pyridine (H 3 L) has been designed, prepared, and employed to synthesize the …

Synthesis of α-l-Threose Nucleoside Phosphonates via Regioselective Sugar Protection

SG Dumbre, MY Jang, P Herdewijn - The Journal of organic …, 2013 - ACS Publications
A new synthesis route to α-l-threose nucleoside phosphonates via 2-O and 3-O selectively
protected l-threose is developed. The key intermediates 2-O-benzoyl-l-threonolactone and 1 …

Efficient convergent synthesis of 1, 3-diazepinone nucleosides by ring-closing metathesis and direct glycosylation

AK Hedger, J Findell, DS Barak, CA Schiffer, JK Watts… - RSC …, 2024 - pubs.rsc.org
A new and highly efficient ring-closing metathesis-based strategy was developed for the
synthesis of the cyclic urea 1, 3-diazepinone, presenting significant improvement upon …

Direct deoxygenation of active allylic alcohols via metal-free catalysis

Q Liu, F Han, H Zhuang, T Zhang, N Ji… - Organic & Biomolecular …, 2022 - pubs.rsc.org
Direct metal-free deoxygenation of highly active allylic alcohols catalyzed by a Brønsted acid
was achieved, which avoids tedious reaction steps and eliminates metal contamination. By …

Nucleosides and Nucleotides. 180. Synthesis and Antitumor Activity of Nucleosides That Have a Hydroxylamino Group Instead of a Hydroxyl Group at the 2 '-or 3 ' …

A Ogawa, M Tanaka, T Sasaki… - Journal of medicinal …, 1998 - ACS Publications
The design and synthesis of potential antitumor antimetabolites 2 '-deoxy-2 '-
(hydroxylamino) uridine (15),-cytidine (19, 2 '-DHAC), and-adenosine (35), their …

Cerium (III) chloride-mediated reactions of sulfonamide dianions

DC Johnson, TS Widlanski - The Journal of Organic Chemistry, 2003 - ACS Publications
Presented here is the first report on the ability of cerium (III) chloride to mediate high-yielding
and, oftentimes, highly diastereoselective additions of N-benzyl-α, N-dilithio …