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Index « FA11s1.i » - entrée « KOZIKOWSKI (A. P.) »
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KOZEL (F. A.) < KOZIKOWSKI (A. P.) < KRA (Renee)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 10.
Ident.Authors (with country if any)Title
004690 (1983) A. P. Kozikowski ; Y. Kitagawa ; J. P. SpringerAn examination of the extent of diastereofacial selection in the reactions of a chiral nitrile oxide with achiral alkenes: a route to β-hydroxy carboxylic acids
004789 (1984) A. P. Kozikowski ; J. G. ScripkoNOC approach to spiroketals: a total synthesis of (±)-talaromycin B
004938 (1984) A. P. Kozikowski ; K. Hiraga ; J. P. Springer ; B. C. Wang ; ZHANG-BAO XU[(4+2)+(3+2)] route to multiply fused ring systems: a new notion in polycycle construction
004991 (1984) A. P. Kozikowski ; K. L. SorgiUse of the anomeric allylation reaction in natural products synthesis ― a stereocontrolled synthesis of methyl deoxypseudomonate B
004A22 (1984) A. P. Kozikowski ; PYEONG-UK PARKSynthesis of 2-substituted Δ3-piperidines: the nitrogen analogue of the Ferrier rearrangement. An approach to streptazolin
004A82 (1984) A. P. Kozikowski ; YON-YIH CHEN ; B. C. Wang ; ZHANG-BAO XUThe intramolecular nitrile oxide cycloaddition (INOC) route to the ergot alkaloids: use of the isoxazoline to γ-amino alcohol conversion in the total synthesis of (+)-paliclavine
004B05 (1984) A. P. Kozikowski ; M. N. GrecoTotal synthesis of the clavicipitic acids by an intramolecular azide cycloaddition strategy
004B61 (1984) A. P. Kozikowski ; A. K. GhoshDiastereofacial selection in nitrile oxide cycloaddition reactions: the anti-directing effect of an allylic oxygen and some new results on the ring metalation of isoxazolines ― A synthesis of (±)-blastmycinone
004C13 (1984) A. P. Kozikowski ; X.-M. ChengA synthesis of 3-substituted pyrroles through the halogen-metal exchange reaction of 3-bromo-1-(triisopropylsilyl)pyrrole
004C46 (1984) A. P. Kozikowski ; P. D. SteinIntramolecular nitrile oxide cycloaddition route to carbocyclics: a formal total synthesis of PGF2α

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