E. Narisano

发表

Enzymes in asymmetric synthesis: Effect of reaction media on the PLE catalysed hydrolysis of diesters

S. Thea, R. Riva, L. Banfi, 1986 .

Acetogenin synthesis. Organocopper reagents, anions of 1,3-dithians and of protected cyanohydrins as intermediates in ketide side-chain synthesis

C. Gennari, C. Scolastico, L. Colombo, 1980 .

A general method for the enantiospecific synthesis of optically active aliphatic sulfenyl chlorides and thiophthalimides

S. Thea, G. Cevasco, E. Narisano, 1990 .

Synthesis of optically pure “open-chain” nucleotide derivatives of asymmetrized tris (hydroxymethyl)methane

V. Merlo, G. Guanti, E. Narisano, 1995 .

Enzymatic preparation of homochiral 2-(n-carbobenzyloxypiperid-4-yl)-1,3-propanediol monoacetate. A facile entry to both enantiomers of 3- hydroxymethylquinuclidine.

S. Brusco, L. Banfi, G. Guanti, 1994 .

Enzyme catalyzed monohydrolysis of 2-aryl-1 3-propanediol diacetates. A study of structural effects of the aryl moiety on the enantioselectivity

S. Thea, Andrew C. Williams, G. Guanti, 1990 .

Chemoenzymatic preparation of a key intermediate for carbapenem synthesis starting from asymmetrized bis(hydroxymethyl)acetaldehyde (BHYMA

L. Banfi, G. Guanti, E. Narisano, 1993 .

Enantiospecific and diastereoselective synthesis of anti α-hydrazino- and α-amino-β-hydroxyacids through “electrophilic amination” of β-hydroxyesters

L. Banfi, G. Guanti, E. Narisano, 1988 .

Diastereoselection in trimethylsilyl trifluoromethanesulphonatecatalyzed reaction of silyl ketene acetals with imines

L. Banfi, G. Guanti, E. Narisano, 1987 .

Enzyme catalysed asymmetrization of pyridyl substituted 1,3-propanediols and of the corresponding diacetates

R. Riva, G. Guanti, E. Narisano, 1997 .

Stereoselective condensation of bis-p-tolylthiomethane with lactic acid derivatives through an acylation–reduction strategy: synthesis of protected 4-deoxy-L-threose and 4-deoxy-L-erythrose

L. Banfi, A. Guaragna, G. Guanti, 1988 .

Enantiospecific synthesis of protected 4-deoxy-L-threose and 4-deoxy-L-erythrose via diastereoselective reduction of l-lactic acid-derived ketones

L. Banfi, G. Guanti, E. Narisano, 1986 .

Microbiological synthesis of variously protected L-glyceraldehydes in high optical purity

L. Banfi, G. Guanti, E. Narisano, 1986 .

Baker's yeast-mediated synthesis of protected α-hydroxy-aldehydes

L. Banfi, A. Guaragna, G. Guanti, 1986 .

Asymmetric synthesis of protected α-hydroxyaldehydes from acyl chlorides using p-tolyl p-tolylthiomethyl sulfoxide as chiral carbonyl synthon

L. Banfi, C. Scolastico, E. Narisano, 1983 .

Chiral acyl anion and enolonium ion equivalents. Asymmetric synthesis of α-methoxy-aldehydes

C. Gennari, C. Scolastico, L. Colombo, 1981 .

Chiral acyl anion equivalents: asymmetric synthesis of α-methoxytolualdehyde

C. Gennari, C. Scolastico, L. Colombo, 1979 .

NEW STEREOSPECIFIC SYNTHESIS OF CHIRAL THIOACETAL MONOSULFOXIDES

L. Colombo, E. Narisano, Cesare Geinnari, 1979 .

Enantiospecific and diastereoselective synthesis of cis monobactams through electrophilic amination of chiral 3-hydroxyesters

R. Riva, L. Banfi, G. Cascio, 1994 .

Asymmetric synthesis of protected α-alkyl-β-amino-δ-hydroxy esters by stereocontrolled elaboration of THYM*

G. Guanti, A. Moro, E. Narisano, 2000 .

Protecting group controlled diastereoselective allylation of asymmetrized bis (hydroxymethyl)acetaldehydes (BHYMA)

L. Banfi, G. Guanti, E. Narisano, 1991 .

A stereocontrolled synthesis of 3-(1′-hydroxyethyl)-2-azetidinones through trimethylsilyl trifluoromethanesulphonate catalyzed condensation of silyl ketene acetal derived from ethyl 3-hydroxybutyrate and imine

L. Banfi, G. Guanti, E. Narisano, 1987 .

Microbiological enantioselective synthesis of (S) and (R) 4-(p-anisyloxy)-3-hydroxybutyrates as new chiral building blocks for the synthesis of β-lactam antibiotics

R. Riva, L. Banfi, C. Ghiron, 1994 .

Dibenzylaminoacetates as useful synthetic equivalents of glycine in the synthesis of α-amino-β-hydroxyacids1

L. Banfi, C. Scolastico, G. Guanti, 1988 .

Monobactams: stereoselective synthesis of trans-3-amino- and 3-acylamino-4-trifluoromethyl-2-azetidinones

E. Bosone, L. Banfi, C. Scolastico, 1985 .

Synthesis of 4-vinyl substituted β-lactams of the oxamazin family

L. Banfi, A. Guaragna, G. Guanti, 1988 .

Enantiospecific and diastereoselective synthesis of C11-C17 fragment of tylonolide from “asymmetrized tris (hydroxymethyl)methane”

L. Banfi, C. Ghiron, G. Guanti, 1991 .

Regiocontrol in reductive ring opening of epoxides derived from asymmetrized 2-alkenyl-1,3-propanediols

L. Banfi, V. Merlo, G. Guanti, 1994 .

9‐O‐(1,2;5,6‐Di‐O‐isopropylidene‐α‐D‐glucofuranosyl)‐9‐boratabicyclo[3.3.1]nonane, Potassium Salt

R. Riva, L. Banfi, E. Narisano, 2001 .

Regiocontrol in nucleophilic ring opening of chiral epoxides of chemoenzymatic origin

V. Merlo, G. Guanti, E. Narisano, 1994 .

Enzymes in organic synthesis: remarkable influence of a π system on the enantioselectivity in PPL catalysed monohydrolysis of 2-substituted 1,3-diacetoxypropanes.

L. Banfi, G. Guanti, E. Narisano, 1990 .

Enzymes as selective reagents in organic synthesis: Enantioselective preparation of “asymmetrized tris (hydroxymethyl)methane”

L. Banfi, G. Guanti, E. Narisano, 1989 .

Enantiospecific and diastereoselective preparation of synthetic equivalents of 2,4-deoxy-2-amino-L-threose and -L-erythrose from (S) ethyl β-hydroxybutyrate. Stereochemical course of their condensations with C-nucleophiles☆

L. Banfi, G. Guanti, E. Narisano, 1989 .

Stereoselective preparation of synthetic equivalents of 2-deoxy-2-amino- and 3-deoxy-3-aminotetroses from malic acid. Application to the synthesis of C18-D-ribo-phytosphingosine

L. Banfi, G. Guanti, E. Narisano, 1989 .

Asymmetrized trils (hydroxymethyl)methane as a highly stereodivergent chiral building block: preparation of all four stereoisomers of protected 2-hydroxymethyl-1,3-butanediol

L. Banfi, G. Guanti, E. Narisano, 1990 .

Electrophilic sulphenylation of silyl ketene acetals derived from 3-hydroxy-esters: diastereoselective synthesis of protected epoxyalcohols

S. Thea, L. Banfi, G. Guanti, 1988 .

Exploitation of highly functionalised epoxides derived from asymmetrized tris(hydroxymethyl)methane (THYM∗) in the synthesis of a fragment of lasalocide A and other related polyether ionofore antibiotics

G. Guanti, E. Narisano, 1996 .

Lipase mediated preparation of differently protected homochiral 2-aryl-2-fluoro-1,3-propanediols

R. Riva, G. Guanti, E. Narisano, 1998 .

Chemoenzymatic synthesis of 2-substituted 2-fluoro-1,3-dioxygenated chiral building blocks

R. Riva, E. Narisano, 1999 .

Stereodivergent Synthesis of cis epoxides derived from asymmetrized 2-alkenyl-1,3-propanediols

S. Thea, L. Banfi, V. Merlo, 1993 .

Stereoselective epoxidation of asymmetrized 2-alkenyl-1,3-propanediols.

S. Thea, L. Banfi, G. Guanti, 1991 .

Stereoselective synthesis of N-acetyl-l-tolyposamine from (S) ethyl β-hydroxybutyrate

R. Riva, L. Banfi, G. Guanti, 1992 .

Asymmetrized Tris (Hydroxymethyl)Methane and Related Synthons as New Highly Versatile Chiral Building Blocks. Chemoenzymatic Preparation and Synthetic Applications

L. Banfi, G. Guanti, E. Narisano, 1992 .

Stereodivergent Synthesis of cis Epoxides Derived from Asymmetrized 2‐ Alkenyl‐1,3‐propanediols.

S. Thea, L. Banfi, V. Merlo, 1994 .

Chemoenzymic preparation of asymmetrized tris(hydroxymethyl)methane (THYM*) and of asymmetrized bis(hydroxymethyl)acetaldehyde (BHYMA*) as new highly versatile chiral building blocks

L. Banfi, G. Guanti, E. Narisano, 1992 .

Acid catalysis in aldol condensation of α-amino silyl ketene acetals. Diastereoselective synthesis of α-amino-β-hydroxyacids.

L. Banfi, C. Scolastico, G. Guanti, 1985 .

Tandem reduction / intramolecular hydroxyalkylation of (3-hydroxyphenyl)alkanoates: a new regioselective approach to 1,8-dihydroxytetralins

S. Thea, R. Riva, L. Banfi, 1992 .