-
1Academic Journal
المؤلفون: David Crich, A. U. Vinod, John Picione, Donald J. Wink
المصدر: ARKIVOC, Vol 2005, Iss 6, Pp 339-344 (2005)
مصطلحات موضوعية: Organic chemistry, QD241-441
وصف الملف: electronic resource
-
2
المؤلفون: Laura Hernandez-Cruz, Charles T. Cox, Thomas A. Holme, Melanie M. Cooper, Ronald H. Stevens, Krystal Buchanan, John Picione, Rebecca Pease
المصدر: Chem. Educ. Res. Pract.. 9:163-168
مصطلحات موضوعية: Performance based assessment, Computer science, business.industry, Educational technology, Education, Online assessment, Engineering management, Software, Chemistry (miscellaneous), Computer software, Management system, The Internet, business, Curriculum, Simulation
-
3
المؤلفون: David Crich, John Picione, Thomas K. Hutton, Abhisek Banerjee, Prasanna Jayalath
المصدر: Tetrahedron: Asymmetry. 16:105-119
مصطلحات موضوعية: Inorganic Chemistry, chemistry.chemical_compound, chemistry, Organic Chemistry, Organic chemistry, Reactivity (chemistry), Glycosyl, Nuclear magnetic resonance spectroscopy, Physical and Theoretical Chemistry, Protecting group, Fluoride, Decomposition, Catalysis
-
4
المؤلفون: Qingjia Yao, John Picione, Mark D. Smith, David Crich
المصدر: Synthesis. 2001:0323-0326
مصطلحات موضوعية: chemistry.chemical_compound, Glycosylation, chemistry, Organic Chemistry, 2,6-Di-tert-butylpyridine, Non-nucleophilic base, Base (exponentiation), Combinatorial chemistry, Catalysis
-
5
المؤلفون: Andy Gill, M. Mahmun Hossain, John Picione, Marion Hilliard, Syed J. Mahmood
المصدر: Tetrahedron Letters. 39:2681-2684
مصطلحات موضوعية: chemistry.chemical_compound, chemistry, Aryl, Yield (chemistry), Organic Chemistry, Drug Discovery, Lewis acids and bases, Ring (chemistry), Biochemistry, Medicinal chemistry, Isomerization, Lewis acid catalysis
-
6
المؤلفون: Marion Hilliard, Andy Gill, Syed J. Mahmood, M. Mahmun Hossain, John Picione
المصدر: ChemInform. 29
مصطلحات موضوعية: chemistry.chemical_compound, Chemistry, Yield (chemistry), Aryl, Organic chemistry, General Medicine, Lewis acids and bases, Ring (chemistry), Medicinal chemistry, Isomerization, Lewis acid catalysis, Diphenylmethane derivatives
-
7
المؤلفون: Qingjia Yao, David Crich, John Picione, Mark D. Smith
المصدر: ChemInform. 32
مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, Glycosylation, chemistry, Base (chemistry), 2,6-Di-tert-butylpyridine, Organic chemistry, General Medicine, Combinatorial chemistry
-
8
المؤلفون: David, Crich, A U, Vinod, John, Picione, Donald J, Wink
المصدر: ARKIVOC : free online journal of organic chemistry. 2005(6)
مصطلحات موضوعية: Article
-
9
المؤلفون: John Picione
المصدر: e-EROS Encyclopedia of Reagents for Organic Synthesis
مصطلحات موضوعية: Solvent, chemistry.chemical_compound, chemistry, Pinacol, Reagent, Pyridine, Organic chemistry, Ether, Solubility, Diethyl ether, Triethylamine
-
10
المؤلفون: John Picione, David Crich
المصدر: ChemInform. 34
مصطلحات موضوعية: Hydrolysis, chemistry.chemical_compound, Aqueous solution, chemistry, Organic Chemistry, Organic chemistry, General Medicine, Piperidine
-
11
المؤلفون: John Picione, David Crich
المصدر: ChemInform. 34
مصطلحات موضوعية: chemistry.chemical_compound, Glycosylation, chemistry, Stereochemistry, General Medicine
-
12
المؤلفون: David Crich, John Picione
المصدر: Organic letters. 5(5)
مصطلحات موضوعية: Sulfonyl, chemistry.chemical_classification, Glycosylation, Organic Chemistry, Biochemistry, Sodium amalgam, Rhamnose, chemistry.chemical_compound, chemistry, Thioglycosides, Organic chemistry, Piperidine, Sulfones, Physical and Theoretical Chemistry, Beta (finance), Pyrans
-
13Academic Journal
المؤلفون: David Crich, A. U. Vinod, John Picione, Donald J. Wink
المصدر: ARKIVOC: vol. 2005, no. 6
Relation: (issn) 1551-7012; (dlps) 5550190.0006.629; (old-style-dlps) 5550190.0006.629; http://hdl.handle.net/2027/spo.5550190.0006.629; (doi) http://dx.doi.org/10.3998/ark.5550190.0006.629; (paper-id) EJ-1580CP; (aleph) 5550190
-
14Dissertation/ Thesis
المؤلفون: John. Picione
Relation: http://hdl.handle.net/10027/12045; https://figshare.com/articles/thesis/Novel_protecting_group_strategies_in_the_direct_stereoselective_formation_of_beta-rhamnopyranosides_/10811225