B. M. HENNESSY - Concepedia

Author

B. M. HENNESSY

Also Known As

B. HENNESSY, B. Hennessy, B. M. HENNESSY, B.M. Hennessy, Bernard Hennessy, Bernard M Hennessy, Bernard M. Hennessy, By E. Hennessy, Hennessy, B.

Publications

558

Citations

H-Index

Concepts

All Affiliations

La Roche College

About

B. M. HENNESSY is an author at La Roche College specializing in pharmacology, chemistry, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	3	3	195
2	Medicine	3	3	134
3	Biochemistry	3	3	77
4	Biomolecular Engineering	3	3	119
5	Natural Sciences	2	2	59

B. M. HENNESSY

Publications

530

Citations

H-Index

Page 1

	Year	Citations
Stereocontrolled total synthesis of 1.alpha.,25-dihydroxycholecalciferol and 1.alpha.,25-dihydroxyergocalciferol Eǹrico G. Baggiolini, Jerome A. Iacobelli, B. M. HENNESSY, The Journal of Organic Chemistry Molecular SciencesAugust 1Altmetric Attention ScoreTotal SynthesisOrganic Chemistry	1986	226
Stereoselective total synthesis of 1.alpha.,25-dihydroxycholecalciferol Eǹrico G. Baggiolini, Jerome A. Iacobelli, B. M. HENNESSY, Journal of the American Chemical Society Chemical MeasurementEngineeringDonut IconStereoselective Total SynthesisMedicine	1982	106
Stereoselective total synthesis of 1α,25S,26-trihydroxycholecalciferol Peter M. Wovkulich, F. Barcelos, Andrew D. Batcho, Tetrahedron Bioorganic ChemistryEngineeringStereoselective Total SynthesisOrganic ChemistryStereoselective Synthesis	1984	76
Stereospecific synthesis of the lythgoe's ring a aldehyde for the preparation of 1α-hdroxylated tachysterols and calciferols Eǹrico G. Baggiolini, B. M. HENNESSY, Jerome A. Iacobelli, Tetrahedron Letters Bioorganic ChemistryStereospecific SynthesisBiochemistryNatural SciencesStereoselective Synthesis	1987	30
Total synthesis of 1.alpha.,25(R)-dihydroxy vitamin D3 26, 23(S)-lactone (calcitriol lactone), a natural metabolite of vitamin D3 Peter M. Wovkulich, Eǹrico G. Baggiolini, B. M. HENNESSY, The Journal of Organic Chemistry Bioorganic ChemistryBiochemistryVitamin D3Natural SciencesVitamin D3 26	1983	29
(25 <i>S</i>)‐1α, 25, 26‐Trihydroxycholecalciferol, a New Vitamin D<sub>3</sub> Metabolite: Synthesis and Absolute Stereochemistry at C(25) John J. Partridge, S.-J. Shiuey, Naresh K. Chadha, Helvetica Chimica Acta Natural Product SynthesisBiochemistryMedicineBioanalysisBovine Serum	1981	18
ChemInform Abstract: Stereocontrolled Total Synthesis of 1α,25‐Dihydroxycholecalciferol (Ia) and 1α,25‐Dihydroxyergocalciferol (Ib). Eǹrico G. Baggiolini, Jerome A. Iacobelli, B. M. HENNESSY, ChemInform EngineeringTotal SynthesisOrganic ChemistryStereoselective SynthesisChemistry	1987	13
Total synthesis of 25-Hydroxy-16,23E-diene Vitamin D3 and 1α,25-Dihydroxy-16,23E-diene Vitamin D3: separation of genomic and nongenomic vitamin D Activities Marek M. Kabat, Walter Burger, Sandra E. Guggino, Bioorganic & Medicinal Chemistry	1998	12
Synthesis and stereochemistry of perhydrobenzo[b]thiophene derivatives Pat N. Confalone, Eǹrico G. Baggiolini, B. M. HENNESSY, The Journal of Organic Chemistry Derivative (Chemistry)Molecular SciencesDerivativesHeterocyclicDonut Icon	1981	10
Potent, selective MCH-1 receptor antagonists Shawn D. Erickson, Bruce L. Banner, Steven J. Berthel, Bioorganic & Medicinal Chemistry Letters Functional SelectivityMedicineReceptor (Biochemistry)PharmacotherapyNon-peptide Ligand	2008	10

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