Eric Block

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Eric Block
Eric Block photograph2.jpg
Eric Block
Born (1942-01-25) January 25, 1942 (age 81)
Nationality American
Alma mater Queens College of the City University of New York (B.S.), Harvard University (M.S., Ph.D.)
Known for Organosulfur chemistry
Allium chemistry
Olfaction chemistry
Awards Guggenheim Fellowship
Ernest Guenther Award
Kenneth A. Spencer Award
Sterling B. Hendricks Memorial Lectureship Award
Fellow of the American Chemical Society
Scientific career
Fields Chemistry
Institutions University at Albany, SUNY
University of Missouri-Saint Louis
Doctoral advisor Elias James Corey
Notes
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Eric Block (born January 25, 1942) is an American chemist whose research has focused on the chemistry of organosulfur and organoselenium compounds, Allium chemistry (the chemistry of garlic, onion, and other alliums), and the chemistry of olfaction. As of 2018, he is Distinguished Professor of Chemistry Emeritus at the University at Albany, SUNY.

Contents

Biography

Eric Block was born in New York City in 1942. He received his B.S. (1962) degree from Queens College of the City University of New York, where he was elected to Phi Beta Kappa. After a research assistant position at Brookhaven National Laboratories he attended Harvard University, where he received his M.S. (1964), and Ph.D. (1967) degrees as both a National Science Foundation and National Institutes of Health Predoctoral Fellow, working with E. J. Corey as a graduate student in the area of organic synthesis using organosulfur compounds. After a postdoctoral fellowship at Harvard with E. J. Corey, Block joined the faculty at the University of Missouri–St. Louis in 1967, becoming Professor in 1979. In 1981, he moved to the University at Albany, SUNY, where he was Chair of Chemistry from 1985–1991. He was named Distinguished Professor in 2002 and Carla Rizzo Delray Professor in 2006. In 2018 he became Emeritus Professor at Albany and Visiting Professor in the Chemistry Department at University of California, Irvine.

Block has also held visiting positions at the Harvard University (1974), University of Bologna (1984), Weizmann Institute (2000), Wolfson College, University of Cambridge (2006), Chinese Academy of Sciences (2013), and University of California, Los Angeles (2018).

Research areas

Block is known for his research on organosulfur and organoselenium chemistry, particularly that of genus Allium plants, such as garlic and onion. This work is summarized in two monographs, two review articles, and is the subject of a 2014 American Chemical Society Webinar. [1] Block's monograph on alliums [2] has been published in a Chinese edition. Since 2005, another major area of collaborative research with neurobiology and computational chemistry colleagues has been the study of the molecular basis for olfaction, particularly the role of metals such as copper in olfaction and molecular mechanisms for sensing thiols [3] as well as musk, such as muscone. With his collaborators Block has also examined the plausibility of the controversial vibration theory of olfaction, reaching the conclusion that it is implausible. [4] [5]

Service

Since 1994, Block has been an editorial board member of the Journal of Agricultural and Food Chemistry . [6] Block also served as associate editor (1984–1988) and editorial board member (1984–2000), for Phosphorus, Sulfur, Silicon and the Related Elements, as editorial board member and founding member of Heteroatom Chemistry, 1990–1995, [7] and as associate editor for Organic Reactions, Volume 30. [8] Block was a founding member and international advisory board member of the International Conference on Heteroatom Chemistry (ICHAC) series of meetings, [9] and Chair of ICHAC-2, held in Albany, NY in 1989. [10] [11] He was also Chair of the Symposium on New Organosulfur Chemistry, Pacifichem 2015 in Honolulu, HI.

Honors and awards

Selected publications

Block has published five books and 257 articles; his books and several of his most cited and recent papers are listed below.

Books
Reviews
Research papers

Related Research Articles

<span class="mw-page-title-main">Garlic</span> Species of edible plant

Garlic is a species of bulbous flowering plant in the genus Allium. Its close relatives include the onion, shallot, leek, chive, Welsh onion, and Chinese onion. It is native to South Asia, Central Asia and northeastern Iran and has long been used as a seasoning worldwide, with a history of several thousand years of human consumption and use. It was known to ancient Egyptians and has been used as both a food flavoring and a traditional medicine. China produced 73% of the world's supply of garlic in 2021.

<span class="mw-page-title-main">Onion</span> Bulbous vegetable, grown for food

An onion, also known as the bulb onion or common onion, is a vegetable that is the most widely cultivated species of the genus Allium. The shallot is a botanical variety of the onion which was classified as a separate species until 2011. Its close relatives include garlic, scallion, leek, and chive.

<span class="mw-page-title-main">Allicin</span> Chemical compound

Allicin is an organosulfur compound obtained from garlic. When fresh garlic is chopped or crushed, the enzyme alliinase converts alliin into allicin, which is responsible for the aroma of fresh garlic. Allicin is unstable and quickly changes into a series of other sulfur-containing compounds such as diallyl disulfide. Allicin is an antifeedant, i.e. the defense mechanism against attacks by pests on the garlic plant.

<span class="mw-page-title-main">Olfactory receptor</span> Chemoreceptors expressed in cell membranes of olfactory receptor neurons

Olfactory receptors (ORs), also known as odorant receptors, are chemoreceptors expressed in the cell membranes of olfactory receptor neurons and are responsible for the detection of odorants which give rise to the sense of smell. Activated olfactory receptors trigger nerve impulses which transmit information about odor to the brain. These receptors are members of the class A rhodopsin-like family of G protein-coupled receptors (GPCRs). The olfactory receptors form a multigene family consisting of around 400 genes in humans and 1400 genes in mice.

<span class="mw-page-title-main">Aroma compound</span> Chemical compound that has a smell or odor

An aroma compound, also known as an odorant, aroma, fragrance or flavoring, is a chemical compound that has a smell or odor. For an individual chemical or class of chemical compounds to impart a smell or fragrance, it must be sufficiently volatile for transmission via the air to the olfactory system in the upper part of the nose. As examples, various fragrant fruits have diverse aroma compounds, particularly strawberries which are commercially cultivated to have appealing aromas, and contain several hundred aroma compounds.

<span class="mw-page-title-main">Ajoene</span> Chemical compound

Ajoene is an organosulfur compound found in garlic (Allium sativum) extracts. It is a colorless liquid that contains sulfoxide and disulfide functional groups. The name (and pronunciation) is derived from "ajo", the Spanish word for garlic. It is found as a mixture of up to four stereoisomers, which differ in terms of the stereochemistry of the central alkene (E- vs Z-) and the chirality of the sulfoxide sulfur (R- vs S-).

<span class="mw-page-title-main">Docking theory of olfaction</span>

The docking theory of olfaction proposes that the smell of an odorant molecule is due to a range of weak non-covalent interactions between the odorant [a ligand] and one or more G protein-coupled odorant receptors. These include intermolecular forces, such as dipole-dipole and Van der Waals interactions, as well as hydrogen bonding. More specific proposed interactions include metal-ion, ion-ion, cation-pi and pi-stacking. Interactions can be influenced by the hydrophobic effect. Conformational changes can also have a significant impact on interactions with receptors, as ligands have been shown to interact with ligands without being in their conformation of lowest energy.

The vibration theory of smell proposes that a molecule's smell character is due to its vibrational frequency in the infrared range. This controversial theory is an alternative to the more widely accepted docking theory of olfaction, which proposes that a molecule's smell character is due to a range of weak non-covalent interactions between its protein odorant receptor, such as electrostatic and Van der Waals interactions as well as H-bonding, dipole attraction, pi-stacking, metal ion, Cation–pi interaction, and hydrophobic effects, in addition to the molecule's conformation.

Organosulfur chemistry is the study of the properties and synthesis of organosulfur compounds, which are organic compounds that contain sulfur. They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin. Nature is abound with organosulfur compounds—sulfur is vital for life. Of the 20 common amino acids, two are organosulfur compounds, and the antibiotics penicillin and sulfa drugs both contain sulfur. While sulfur-containing antibiotics save many lives, sulfur mustard is a deadly chemical warfare agent. Fossil fuels, coal, petroleum, and natural gas, which are derived from ancient organisms, necessarily contain organosulfur compounds, the removal of which is a major focus of oil refineries.

Luca Turin is a biophysicist and writer with a long-standing interest in bioelectronics, the sense of smell, perfumery, and the fragrance industry.

<span class="mw-page-title-main">Thial</span> Chemical group (–CH=S)

In organic chemistry, a thial or thioaldehyde is a functional group which is similar to an aldehyde, RC(O)H, in which a sulfur (S) atom replaces the oxygen (O) atom of the aldehyde. Thioaldehydes are even more reactive than thioketones. Unhindered thioaldehydes are generally too reactive to be isolated — for example, thioformaldehyde, H2C=S, condenses to the cyclic trimer 1,3,5-trithiane. Thioacrolein, H2C=CHCH=S, formed by decomposition of allicin from garlic, undergoes a self Diels-Alder reaction giving isomeric vinyldithiins. While thioformaldehyde is highly reactive, it is found in interstellar space along with its mono- and di-deuterated isotopologues. With sufficient steric bulk, however, stable thioaldehydes can be isolated.

<span class="mw-page-title-main">Diallyl disulfide</span> Chemical compound

Diallyl disulfide is an organosulfur compound derived from garlic and a few other genus Allium plants. Along with diallyl trisulfide and diallyl tetrasulfide, it is one of the principal components of the distilled oil of garlic. It is a yellowish liquid which is insoluble in water and has a strong garlic odor. It is produced during the decomposition of allicin, which is released upon crushing garlic and other plants of the family Alliaceae. Diallyl disulfide has many of the health benefits of garlic, but it is also an allergen causing garlic allergy. Highly diluted, it is used as a flavoring in food. It decomposes in the human body into other compounds such as allyl methyl sulfide.

Tetrahydrothiophene is an organosulfur compound with the formula (CH2)4S. The molecule consists of a five-membered saturated ring with four methylene groups and a sulfur atom. It is the saturated analog of thiophene. It is a volatile, colorless liquid with an intensely unpleasant odor. It is also known as thiophane, thiolane, or THT.

<span class="mw-page-title-main">Sulfenic acid</span> Organosulfur compound of the form R–SOH

In chemistry, a sulfenic acid is an organosulfur compound and oxoacid with the general formula R−S−OH. It is the first member of the family of organosulfur oxoacids, which also include sulfinic acids and sulfonic acids, respectively. The base member of the sulfenic acid series with R = H is hydrogen thioperoxide.

<i>syn</i>-Propanethial-<i>S</i>-oxide Chemical compound

syn-Propanethial S-oxide (or (Z)-propanethial S-oxide), a member of a class of organosulfur compounds known as thiocarbonyl S-oxides (formerly "sulfines"), is a volatile liquid that acts as a lachrymatory agent (triggers tearing and stinging on contact with the eyes). The chemical is released from onions, Allium cepa, as they are sliced. The release is due to the breaking open of the onion cells and their releasing enzymes called alliinases, which then break down amino acid sulfoxides, generating sulfenic acids. A specific sulfenic acid, 1-propenesulfenic acid, formed when onions are cut, is rapidly rearranged by a second enzyme, called the lachrymatory factor synthase or LFS, giving syn-propanethial S-oxide. The gas diffuses through the air and, on contact with the eye, it stimulates sensory neurons creating a stinging, painful sensation. Tears are released from the tear glands to dilute and flush out the irritant. A structurally related lachrymatory compound, syn-butanethial S-oxide, C4H8OS, has been found in another genus Allium plant, Allium siculum.

<span class="mw-page-title-main">OR1A1</span> Protein-coding gene in the species Homo sapiens

Olfactory receptor 1A1 is a protein that in humans is encoded by the OR1A1 gene.

<span class="mw-page-title-main">Thietane</span> Chemical compound

Thietane is a heterocyclic compound containing a saturated four-membered ring with three carbon atoms and one sulfur atom.

<i>Allium stipitatum</i> Species of flowering plant

Allium stipitatum, Persian shallot, is an Asian species of onion native to central and southwestern Asia.

<i>Allium</i> Genus of flowering plants in the family Amaryllidaceae

Allium is a genus of monocotyledonous flowering plants with hundreds of species, including the cultivated onion, garlic, scallion, shallot, leek, and chives. The generic name Allium is the Latin word for garlic, and the type species for the genus is Allium sativum which means "cultivated garlic".

<span class="mw-page-title-main">Selenosulfide</span>

In chemistry, a selenosulfide refers to distinct classes of inorganic and organic compounds containing sulfur and selenium. The organic derivatives contain Se-S bonds, whereas the inorganic derivatives are more variable.

References

  1. "Garlic and Other Alliums: The Lore and the Science - American Chemical Society". American Chemical Society. Archived from the original on 2016-05-14. Retrieved 2018-05-15.
  2. McGee, Harold (2010-06-08). "The Chemical Weapons of Onions and Garlic". The New York Times.
  3. "Copper key to our sensitivity to rotten eggs' foul smell". chemistryworld.com. Archived from the original on 10 May 2017. Retrieved 3 May 2018.
  4. Everts, S. (2015). "Receptor research reignites a smelly debate". Chem. Eng. News. 93 (18): 29–30.
  5. Vosshall, L. B. (2015). "Laying a controversial smell theory to rest". Proc. Natl. Acad. Sci. USA. 112 (21): 6525–6526. Bibcode:2015PNAS..112.6525V. doi: 10.1073/pnas.1507103112 . PMC   4450429 . PMID   26015552.
  6. "Editorial Board". pubs.acs.org.
  7. "Masthead". Heteroatom Chemistry. 1 (6): fmi. 1 December 1990. doi: 10.1002/hc.520010601 .
  8. "Olefin Synthesis via Deoxygenation of Vicinal Diols - Organic Reactions Wiki". organicreactions.org. Archived from the original on 2022-10-23. Retrieved 2018-06-03.
  9. "ICHAC 2017". groups.chem.ubc.ca.
  10. Ohno, Atsuyoshi (3 June 2018). "In memory of the late Professor Shigeru Oae". Heteroatom Chemistry. 13 (5): 388–389. doi: 10.1002/hc.10071 .
  11. "ICHAC". www.unioviedo.es.[ permanent dead link ]
  12. "John Simon Guggenheim Foundation | Eric Block". Gf.org. 2014-06-20. Retrieved 2018-06-03.
  13. 1 2 "Awards" (PDF). agfd.sites.acs.org. Archived from the original (PDF) on 2020-07-21. Retrieved 2018-06-03.
  14. "Spencer Award History". Kansas City Local Section.[ permanent dead link ]
  15. "2012 Sterling B. Hendricks Memorial Lectureship - AGRO Division". www.agrodiv.org.[ permanent dead link ]
  16. "Block, Eric". 1 August 2016.[ permanent dead link ]
  17. "2014 ACS Fellows - American Chemical Society". American Chemical Society.
  18. "Ernest Guenther Award in the Chemistry of Natural Products - American Chemical Society". American Chemical Society.
  19. "2018 Christopher S. Foote Lecture - UCLA Chemistry and Biochemistry". www.chemistry.ucla.edu.