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- Currently displaying 761 - 780 of 1019 publications
Tuning the Reactivity of Glycosides: Efficient One-pot Oligosaccharide Synthesis1
Synlett
(1995)
1995
781
(doi: 10.1055/s-1995-5052)
Chemistry of insect antifeedants from Azadirachta Indica (Part 19): 1A potential relay route for the synthesis of azadirachtin
Tetrahedron
(1995)
51
6591
(doi: 10.1016/0040-4020(95)00297-l)
BIOSYNTHESIS OF TETRONASIN .4. PREPARATION OF DEUTERIUM-LABELED C19-C26, C17-C26, C-11-C26 AND C3-C26 POLYKETIDE FRAGMENTS AS PUTATIVE BIOSYNTHETIC PRECURSORS OF THE IONOPHORE ANTIBIOTIC TETRONASIN (ICI-139603)
Tetrahedron
(1995)
51
5417
(doi: 10.1016/0040-4020(95)00201-I)
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .18. DEMETHYLATION AND METHYLATION OF THE C-8 POSITION OF THE DECALIN PORTION OF AZADIRACHTIN
Tetrahedron
(1995)
51
2077
(doi: 10.1016/0040-4020(94)01071-7)
Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex
Chemical Communications
(1995)
1751
(doi: 10.1039/c39950001751)
Behavioural responses of locusts and Spodoptera littoralis to azadirachtin and azadirachtin analogues containing fluorescent and immunogenic reporter groups
Journal of Insect Physiology
(1995)
41
555
(doi: 10.1016/0022-1910(95)00014-l)
Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols.
Tetrahedron Asymmetry
(1995)
6
2403
(doi: 10.1016/0957-4166(95)00318-J)
DISPIROKETALS IN SYNTHESIS .14. FUNCTIONALIZED DISPIROKETALS AS NEW CHIRAL AUXILIARIES - HIGHLY STEREOSELECTIVE MICHAEL ADDITIONS TO A BIFUNCTIONAL, C-2-SYMMETRICAL CHIRAL AUXILIARY
Tetrahedron Letters
(1994)
35
7455
(doi: 10.1016/0040-4039(94)85340-1)
Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary
Tetrahedron Letters
(1994)
35
7451
(doi: 10.1016/0040-4039(94)85339-8)
Dispiroketals in synthesis (Part 11): Concomitant enantioselective and regioselective protection of 2,5- dibenzoyl-myo-inositol
Tetrahedron Letters
(1994)
35
7443
(doi: 10.1016/0040-4039(94)85337-1)
Dispiroketals in synthesis (Part 12): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form
Tetrahedron Letters
(1994)
35
7447
(doi: 10.1016/0040-4039(94)85338-X)
SELECTIVE ACYLATION AND ALKYLATION REACTIONS OF DIOLS USING DIBUTYLTIN DIMETHOXIDE (PG 913, 1993)
SYNLETT
(1994)
764
Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues
FEMS Microbiology Letters
(1994)
120
267
(doi: 10.1016/0378-1097(94)90482-0)
Model studies towards the insect antifeedant Jodrellin A using an organoselenium mediated cyclization reaction
Tetrahedron Letters
(1994)
35
4861
Studies towards the total synthesis of rapamycin: A convergent and stereoselective synthesis of the C22C32 carbon framework
Tetrahedron Letters
(1994)
35
2087
STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - PREPARATION OF THE C10-C17 CARBON UNIT
Tetrahedron Letters
(1994)
35
2095
Studies towards the total synthesis of rapamycin: Preparation of the cyclohexyl C33C42 fragment and further coupling to afford the C22C42 carbon unit
Tetrahedron Letters
(1994)
35
2091
DISPIROKETALS IN SYNTHESIS .6. HIGHLY STEREOSELECTIVE ALKYLATION OF DISPIROKETAL PROTECTED LACTATE AND GLYCOLATE ENOLATES
Tetrahedron Letters
(1994)
35
769
TOWARDS THE SYNTHESIS OF THE C-37-C-42 FRAGMENT OF RAPAMYCIN - INTRAMOLECULAR REACTIONS OF ALLYL SILANES WITH OXONIUM IONS GENERATED FROM ALPHA-ALKOXY SULFONES
Tetrahedron
(1994)
50
835
Two new routes to the C19C26 tetrahydrofuran fragment of the acyl tetronic acid ionophore tetronasin (ICI M139603)
Tetrahedron Letters
(1994)
35
319