998 results on '"Servi, S"'
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152. ChemInform Abstract: Biogeneration of Aromas
153. ChemInform Abstract: The Enzymatic Preparation of (2R,3S)-Phenyl Glycidic Acid Esters.
154. ChemInform Abstract: Microbial Generation of (2R,3S)- and (2S,3S)-Ethyl 2-Benzamidomethyl-3- hydroxybutyrate, a Key Intermediate in the Synthesis of (3S,1′R)-3-(1′- Hydroxyethyl)azetidin-2-one.
155. ChemInform Abstract: Stereochemistry of Baker′s Yeast Mediated Reduction of α,β- Unsaturated δ-Lactones in the Goniothalamin Series.
156. ChemInform Abstract: Phospholipase D from Streptomyces Catalyses the Transfer of Secondary Alcohols.
157. ChemInform Abstract: Baker′s Yeast Reduction of Arylidenecycloalkanones.
158. ChemInform Abstract: Bakers′ Yeast-Mediated Synthesis of (R)-Aminoglutethimide.
159. ChemInform Abstract: Microbially-Aided Preparation of (S)-2-Methoxycyclohexanone Key Intermediate in the Synthesis of Sanfetrinem.
160. ChemInform Abstract: Stereochemistry of the Baeyer-Villiger Degradation of Aryl Alkyl Ketones Structurally Related to Raspberry Ketone by Beauveria bassiana.
161. ChemInform Abstract: Preparative Transformation of Natural Phospholipids Catalyzed by Phospholipase D from Streptomyces.
162. ChemInform Abstract: Enzyme-Mediated Synthesis of Two Diastereoisomeric Forms of Phosphatidylglycerol and of Diphosphatidylglycerol (Cardiolipin).
163. ChemInform Abstract: A Strategy for the Transformation of a Multifunctional Chiral Synthon of Moderate e.e. into an Enantiomerically Pure Synthetic Intermediate.
164. Reduction of norepinephrine levels with biventricular pacing but recurrence of arrhythmic events in patients with biventricular-ICD and cardiomyopathy
165. [The usefulness of intravascular echography in interventional cardiology]
166. Ostial and midshaft lesions vs. bifurcation lesions in 1111 patients with unprotected left main coronary artery stenosis treated with drug-eluting stents: results of the survey from the Italian Society of Invasive Cardiology
167. Are drug-eluting stents superior to bare-metal stents in patients with unprotected non-bifurcational left main disease? Insights from a multicentre registry
168. Modificazioni a distanza della funzione ventricolare sinistra dopo angioplastica coronarica: differenza tra pazienti con e senza restenosi
169. A comparison between coronary artery bypass grafting surgery and drug eluting stent for the treatment of unprotected left main coronary artery disease in elderly patients (aged >=75 years)
170. Synthesis, Platelet Adhesion and Cytotoxicity Studies of New Glycerophosphoryl-Containing Polyurethanes
171. Mental stress as a provocative test in patients with various clinical syndromes of coronary artery disease
172. Elastic recoil after PTCA; a predictor of restenosis?
173. Preparation of enantiomerically pure methyl (R)-a-hydroxy(2-furyl)acetate by Baker's yeast reduction in multiphase systems
174. Significance of total and differential leucocyte count in patients with acute myocardial infarction treated with primary coronary angioplasty
175. Investigation of Antioxidant Vitamins (A, E, C) and Lipid Peroxidation Levels in Rats Injected N-(1,3-Benzothiazol-2-yl)-N-(4,5-dihydro-1H-imidazol-2-yl) amine
176. Addition of Organochromium Reagents to Heteroaryl Aldehydes. Synthesis of Heteroaryl Substituted bis-Allyl Ethers and Homoallyl Ethers
177. An Investigation of the Reactions of Substituted Homoallylic Alcohols with Various Oxidation Reagents
178. ChemInform Abstract: Synthesis of Allyl-cyclopropyl Alcohols and Allyl-1,5-hexadien-3-ols and Investigation of Their Antibacterial and Antifungal Activities.
179. Biocatalysis as a useful tool in pheromone synthesis. Enantiomerically pure building blocks from baker's yeast reductions and enzyme catalysed resoluti
180. Old and New Synthetic Capacities of Baker's Yeast
181. Fermenting Bakers' yeast reduction of a-methyl-b-(2-furyl)acrolein
182. Enantioselective Synthesis Of (S)-2-Methyl-1-Alkanols Via Bakers-Yeast Mediated Reduction Of Alpha-Methyl-2-Thiophenepropenals
183. Chiral Amino-alcohols from Baker's Yeast Reduction of Alpha-Keto-acid Derivatives
184. Phenotype characterization of circulating lymphocytes in ischemic heart disease
185. Factors affecting the therapeutic choice in patients with multivessel coronary artery disease. The Studio Lombardo Angiografia Multivasali (SLAM) Study Group.
186. ChemInform Abstract: Indirect Enzymatic Phosphorylation: Preparation of Dihydroxyacetone Phosphate.
187. Effect of the increasing use of coronary angioplasty on outcome at one year in patients with unstable angina.
188. Resurrecting coronary angioplasty in acute myocardial infarction
189. ChemInform Abstract: Reduction of Carboxylates to Alkanols Catalyzed by Colletotrichum gloeosporoides.
190. Influence of plaque morphology on the mechanism of luminal enlargement after directional coronary atherectomy and balloon angioplasty.
191. Trapidil (triazolopyrimidine), a platelet-derived growth factor antagonist, reduces restenosis after percutaneous transluminal coronary angioplasty. Results of the randomized, double-blind STARC study. Studio Trapidil versus Aspirin nella Restenosi Coronarica.
192. Biocatalysis as a useful tool in pheromone synthesis. Enantiomerically pure building blocks from baker's yeast reductions and enzyme catalysed resoluti
193. Old and New Synthetic Capacities of baker's Yeast
194. ChemInform Abstract: Pen G Acylase Catalyzed Resolution of Phenylacetate Esters of Secondary Alcohols.
195. Increased expression of neutrophil and monocyte adhesion molecules in unstable coronary artery disease.
196. ChemInform Abstract: Chiral Amino Alcohols from Baker′s Yeast Reduction of α‐Keto‐ acid Derivatives.
197. ChemInform Abstract: Enzyme Assisted Synthesis of (S)‐Sotolon (I).
198. Different susceptibility to the development of nitroglycerin tolerance in the arterial and venous circulation in humans. Effects of N-acetylcysteine administration.
199. ChemInform Abstract: Enantioselective Recognition of the Phenacetyl Moiety in the Pen G Acylase‐Catalyzed Hydrolysis of Phenylacetate Esters.
200. Minor synthetic capacities of baker’s yeast towards unnatural substrates
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