Enantioselective Synthesis of Alkaloids and Carbohydrates via
Chemoenzymatic Methods.
T. Hudlicky, Pure Appl. Chem., 1994, 66, 2067.
Key Words:
Design constraints in practical syntheses of complex molecules: Current
status, case studies with carbohydrates and alkaloids, and future perspectives.
T. Hudlicky, Chem. Rev., 1996, 96, 3.
Key Words:
TANDEM RADICAL CYCLIZATION/COMPUTER-ASSISTED ANALYSIS/ORGANIC-SYNTHESIS/ENANTIODIVERGENT
SYNTHESIS/ASYMMETRIC HYDROGENATION/MICROBIAL OXIDATION/ENANTIOSELECTIVE
SYNTHESIS/TETRACYCLIZATION REACTION/DAPHNIPHYLLUM ALKALOIDS/PYRROLIZIDINE
ALKALOIDS
Natural product synthesis via biocatalysis: An essay on the merits of
multidisciplinary ventures.
T. Hudlicky, Journal of the Brazilian Chemical Society, 1998, 9,
313.
Key Words:
biocatalysis/natural synthesis/IONOMYCIN/ALKALOIDS/CYCLITOLS/STRATEGY/FUTURE
T. Hudlicky, Bentham Science Publishers, Hilversum, The Netherlands, 1998.
Key Words:
Recent progress in efficient syntheses of Amaryllidaceae and morphine
alkaloids.
T. Hudlicky, J. Heterocycl. Chem., 2000, 37, 535.
Key Words:
review Amaryllidaceae morphine alkaloid prepn
T. Hudlicky, G. Butora, S. P. Fearnley, A. G. Gum, M. R. Stabile, in Studies
in Natural Products Chemistry, Vol 18 (Ed.: A. U. Rahman), Elsevier Science
Publ B V, Sara Burgerhartstraat 25/PO Box 211/1000 AE Amsterdam/Netherlands, 1996,
pp. 43.
Key Words:
T. Hudlicky, M. Cehulak, Cyclitols and Their Derivatives: A Handhook of
Physical, Spectral, and Synthetic Data., VCH, New York, 1993.
Key Words:
Modern methods of monosaccharide synthesis from non-carbohydrate sources.
T. Hudlicky, D. A. Entwistle, K. K. Pitzer, A. J. Thorpe, Chem. Rev., 1996,
96, 1195.
Key Words:
PSEUDO-BETA-D/ENZYME-CATALYZED SYNTHESIS/DERIVATIVES NAKED SUGARS/CYCLO-ADDITION
REACTION/ALPHA-D-GLUCOPYRANOSE/DIELS-ALDER REACTION/ONE-STEP SYNTHESIS/CMP-SIALIC
ACID/MICROBIAL OXIDATION/STEREOSELECTIVE SYNTHESIS
Enzymic hydroxylation of arene and symmetry considerations in efficient
synthetic design of oxygenated natural products.
T. Hudlicky, R. Fan, H. Luna, H. Olivo, J. Price, Pure Appl. Chem., 1992,
64, 1109.
Key Words:
Divinylcyclopropane-cycloheptadiene rearrangement.
T. Hudlicky, R. Fan, J. Reed, K. G. Gadamasetti, Org. React. (N.Y.), 1992,
41, 1.
Key Words:
Enzymatic Dihydroxylation of Aromatics in Enantioselective Synthesis:
Expanding Asymmetric Methodology.
T. Hudlicky, D. Gonzalez, D. T. Gibson, Aldrichimica Acta, 1999, 32,
35.
Key Words:
The Vinylcyclopropane-Cyclopentene Rearrangement.
T. Hudlicky, T. M. Kutchan, S. M. Naqvi, Org. React. (N.Y.), 1985,
33, 247.
Key Words:
C-C BOND FORMATION/ANNULATIONS/5-RING/EXPANSION/PHYSICAL ORGANIC/REARRANGEMENTS
T. Hudlicky, M. G. Natchus, in Organic Synthesis: Theory and Applications
(Ed.: T. Hudlicky), Jai Press, Greenwich, CT, 1993.
Key Words:
Anionic Approaches to the Construction of Cyclopentanoids.
T. Hudlicky, S. D. Price, Chem. Rev., 1989, 89, 1467.
Key Words:
C-C BOND FORMATION/ANNULATIONS/5-RING/CYCLOPROPANE CLEAVAGE/ALDOL/WITTIG/FAVORSKII/RAMBERG-BACKLUND/NAZAROV/CARBOMETALLATION/Mg/RING
CONTRACTION/6 TO 5
T. Hudlicky, J. W. Reed, in Comprehensive Organic Synthesis, Vol. 5
(Eds.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, p. 899.
Key Words:
C-C BOND FORMATION/PERICYCLIC REACTIONS/SIGMATROPIC/[1/3]
T. Hudlicky, J. W. Reed, in Advances in Asymmetric Synthesis, Vol. 1
(Ed.: A. Hassner), Jai Press Inc, Greenwich, CT, 1995, pp. 271.
Key Words:
Current status and future perspectives of cyclohexadiene-cis-diols in organic
synthesis: Versatile intermediates in the concise design of natural products.
T. Hudlicky, A. J. Thorpe, J. Chem. Soc., Chem. Commun., 1996,
1993.
Key Words:
PSEUDOMONAS-PUTIDA ML2/DIELS-ALDER REACTIONS/MICROBIAL OXIDATION/ENANTIOCONTROLLED
SYNTHESIS/ENANTIODIVERGENT SYNTHESIS/ENANTIOSELECTIVE SYNTHESIS/ANTINEOPLASTIC
AGENTS/ENZYMATIC ASYMMETRIZATION/ENANTIOSPECIFIC SYNTHESIS/CHEMOENZYMATIC
SYNTHESIS
An Overview of the Total Synthesis of Pyrrolizidine Alkaloids via
[4+1]Azide-Diene Annulation Methodology.
T. Hudlicly, G. Seoane, J. D. Price, K. G. Gadamasetti, Synlett, 1990,
433.
Key Words: