L. L. HUCKSTEP - Concepedia

Author

L. L. HUCKSTEP

Eli Lilly (United States)

Also Known As

L. Huckstep, L. L. HUCKSTEP, L. L. Huckstep, L.L. Huckstep, Lyell L. Huckstep

Publications

532

Citations

H-Index

Concepts

All Affiliations

Eli Lilly (United States)

About

L. L. HUCKSTEP is an author at Eli Lilly (United States) specializing in biochemistry, medicine, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	10	10	359
2	Medicine	8	8	274
3	Natural Sciences	8	8	238
4	Engineering	4	4	170
5	Biology	1	1	17

L. L. HUCKSTEP

Publications

465

Citations

H-Index

Page 1

	Year	Citations
Aranotin and related metabolites from Arachniotus aureus. I. Determination of structure R. Nagarajan, L. L. HUCKSTEP, David H. Lively, Journal of the American Chemical Society Pharmaceutical ScienceBiosynthesisEngineeringBiochemistryMedicine	1968	105
Aranotin and related metabolites. II. Isolation, characterization, and structures of two new metabolites Norbert Neuss, R. Nagarajan, Bryan B. Molloy, Tetrahedron Letters Chemical BiologyBiochemistryNatural SciencesSecondary MetaboliteNatural Product Biosynthesis	1968	60
Use of chiral isopropyl groups in biosynthesis. Synthesis of (2RS,3S)-[413C]-valine Jack E. Baldwin, J. Loeliger, William H. Rastetter, Journal of the American Chemical Society BiosynthesisBioorganic ChemistryEngineeringBiochemistryNatural Sciences	1973	37
A NEW DIPEPTIDE ANTIBIOTIC FROM STREPTOMYCES COLLINUS, LINDENBEIN Bryan B. Molloy, David H. Lively, Richard M. Gale, The Journal of Antibiotics	1972	35
Vinca alkaloids. XXX. Chemistry of the deoxyvinblastines (deoxy-vlb), leurosine (vlr), and pleurosine, dimeric alkaloids from linn. ( G. Don) Norbert Neuss, Marvin Gorman, Nancy J. Cone, Tetrahedron Letters Molecular PharmacologyPharmaceutical ChemistryBioorganic ChemistryVinca AlkaloidsBiochemistry	1968	34
The Use of <sup>13</sup>C–NMR. Spectroscopy in Biosynthetic Studies. II[1]. Biosynthesis of narasin, a new polyether ionophore from fermentation of <i>Streptomyces aureofaciens</i> [2] Douglas E. Dorman, Jonathan W. Paschal, Walter M. Nakatsukasa, Helvetica Chimica Acta C‐labeled AcetateBiosynthetic StudiesMicrobial PhysiologyPolyether IonophoreBiosynthesis	1976	30
Vinca alkaloids. XXIX. Structure of leurosidine (vinrosidine, VRD), an oncolytic alkaloid from linn. ( G. Don) Norbert Neuss, L. L. HUCKSTEP, Nancy J. Cone Tetrahedron Letters Medicinal ChemistryPharmaceutical ChemistryBioorganic ChemistryVinca AlkaloidsBiochemistry	1967	25
High performance liquid chromatography (HPLC) of natural products. V. The use of HPLC in the cell-free biosynthetic conversion of .ALPHA.-aminoadipyl-cysteinyl-valine (LLD) into isopenicillin N. Norbert Neuss, D. M. BERRY, Jutta Kupka, The Journal of Antibiotics	1982	24
Vinca alkaloids XXXV. Desacetoxyvinblastine a new minor alkaloid fromVinca rosea L. (Catharanthus roseus G. Don) Norbert Neuss, Albert J. Barnes, L. L. HUCKSTEP Cellular and Molecular Life Sciences Bioorganic ChemistryMedicineHerbal MedicineSecondary MetabolitePhytopharmacology	1975	24
<i>Vinca</i> Alkaloids XXXIII [1]. Microbiological Conversions of Vincaleukoblastine (VLB, Vinblastine), an Antitumor Alkaloid from <i>Vinca rosea</i>. L<scp>INN</scp> Norbert Neuss, G. E. Mallett, D. R. Brannon, Helvetica Chimica Acta Chemical TransformationMicrobiological ConversionsSecondary MetaboliteHydroxy VlbChemistry	1974	23

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