Identification of Azadirachtin in Tissue-Cultured Cells of Neem (Azadirachta Indica)
Natural Product Research
(1997)
10
95
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A General C-Glycosidation Procedure via Anomeric Oxygen to Carbon Rearrangements of Tetrahydropyranyl Ether Derivatives
Synlett
(1997)
1997
1055
(doi: 10.1055/s-1997-1531)
One-Pot Synthesis of Tetra- and Pentasaccharides from Monomeric Building Blocks Using the Principles of Orthogonality and Reactivity Tuning
Synlett
(1997)
1997
257
(doi: 10.1055/s-1997-765)
Direct protection of 1,2-diols from alpha-diketones (pg 793, 1996)
SYNLETT
(1996)
932
Dispiroketals in synthesis .22. Use of chiral 2,2'-bis(phenylthiomethyl)dihydropyrans as new protecting and resolving agents for 1,2-diols (pg 791, 1996)
SYNLETT
(1996)
932
Chemistry of insect antifeedants from Azadirachta indica (part 21): Synthesis of model compounds of azadirachtin using a decalin framework as a functional group scaffolding
Journal of the Chemical Society, Perkin Transactions 1
(1996)
1523
(doi: 10.1039/p19960001523)
Chemistry of insect antifeedants from Azadirachta indica .20. Synthesis of biologically active, simple analogues of azadirachtin, containing the hydroxytetrahydrofurancarboxylate hemiketal moiety
J CHEM SOC PERK T 1
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1517
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(pi-Allyl)tricarbonyliron Lactone Complexes in Organic Synthesis: A Useful and Conceptually Unusual Route to Lactones and Lactams.
Chemical Reviews
(1996)
96
423
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Synthetic studies towards the clerodane insect antifeedant jodrellin A: Preparation of a polycyclic model compound with antifeedant activity
J. Chem. Soc., Perkin Trans. 1
(1996)
611
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Autoradiographic localization of [22,23-(3)H(2)] dihydroazadirachtin binding sites in desert locust testes and effects of Azadirachtin on sperm motility.
Tissue & cell
(1996)
28
725
Diastereoselective additions to aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes
Chem. Commun.
(1996)
317
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Diastereoselective addition reactions of allylstannanes to carbonyl groups in the side-chain of π-allyltricarbonyliron lactone complexes
Chemical Communications
(1996)
657
(doi: 10.1039/CC9960000657)
Dispiroketals in synthesis .20. Preparation of chiral 2,2'-bis(halomethyl) and 2,2'bis(phenylthiomethyl)dihydropyrans
Synlett
(1996)
1996
787
(doi: 10.1055/s-1996-5520)
Dispiroketals in synthesis .21. Use of chiral 2,2'-bis(halomethyl)dihydropyrans as new protecting and resolving agents for 1,2-diols
Synlett
(1996)
1996
789
(doi: 10.1055/s-1996-5521)
Dispiroketals in synthesis .22. Use of chiral 2,2'-bis(phenylthiomethyl)-dihydropyrans as new protecting and resolving agents for 1,2-diols
Synlett
(1996)
1996
791
(doi: 10.1055/s-1996-5522)
Dispiroketals: A new functional group for organic synthesis
Journal of the Chemical Society Perkin Transactions 1
(1995)
2
365
(doi: 10.1039/co9950200365)
Spiroketal glycomimetics: the synthesis of a conformationally restrained Sialyl Lewis X mimic
Bioorganic & Medicinal Chemistry Letters
(1995)
5
2637
(doi: 10.1016/0960-894X(95)00469-A)
DISPIROKETALS IN SYNTHESIS .18. REGIOSELECTIVE AND ENANTIOSELECTIVE PROTECTION OF SYMMETRICAL POLYOL SUBSTRATES USING AN ENANTIOPURE (2S,2'S)-DIMETHYL-BIS-DIHYDROPYRAN (SEPTEMBER, PG 898, 1995)
SYNLETT
(1995)
1196
Solid Phase Synthesis of Bicyclo[2.2.2]octane Derivatives via Tandem Michael Addition Reactions and Subsequent Reductive Amination
Synlett
(1995)
1995
1017
(doi: 10.1055/s-1995-5164)
