Ralph Raphael CBE FRS FRSE
Born	Ralph Alexander Raphael (1921-01-01)1 January 1921 Croydon, London, England
Died	27 April 1998(1998-04-27) (aged 77) Cambridge, Cambridgeshire, England
Nationality	British
Alma mater	Imperial College
Known for	Acetylene chemistry, Organic synthesis
Spouse	Prudence Maguerire Anne née Gaffikin
Awards	Meldola Medal(1948) Tilden Medal (1960)
Scientific career
Fields	Organic Chemistry Natural Products
Institutions	Imperial College Glasgow University Queen's University Belfast Cambridge University
Thesis	(1943)
Doctoral advisors	Sir Ewart Jones Sir Ian Heilbron
Doctoral students	A. Ian Scott Robert Ramage

Ralph Alexander Raphael CBE FRS FRSE (1 January 1921 – 27 April 1998) was a British organic chemist, well known for his use of acteylene derivatives in the synthesis of natural products with biological activity.^[1][2]

Ralph Raphael was born in Croydon, London on New Year's Day 1921, the son of master tailor Jacob ("Jack") Raphael (1889-1978) and his wife, Lily (née Woolf; 1892-1956).^[3] He attended secondary school at Wesley College, Dublin and then Tottenham County School, where a chemistry master, Edgar Ware, introduced him to the subject that would become Raphael's lifetime passion. In 1939 he won scholarships to study at Imperial College, graduating BSc with a first-class degree in 1941 and winning the Hofmann Prize for practical chemistry.^[1] During the Second World War both the undergraduate and PhD courses at Imperial College were of two year's duration and Raphael completed the latter in 1943. His doctoral work, aimed at the synthesis of vitamin A, was published in five collaborative papers on the chemistry of acetylenes and that topic became a hallmark of his subsequent research career.^[1][4][5][6]

As a new PhD, Raphael was allocated to the wartime effort on the antibiotic penicillin, working from 1943 to 1946 at the May & Baker laboratories.^[7] After the war, he obtained an ICI fellowship (for 1946–1949) that allowed him to return to Imperial College to pursue independent research: an early highlight was his synthesises of penicillic acid, the major product of acid degradation of penicillin (although not containing its characteristic β-lactam substructure).^[8] Another was his collaboration with Franz Sondheimer on natural products including an insecticide extracted from Zanthoxylum clava-herculis (a diene then called herculin, now systematically named as (2E,8E)-N-isobutyl-2,8-dodecadienamide); work which led to Raphael's award of the Meldola Medal in 1948.^[1][6] In 1949, Raphael was appointed to his first permanent job, as a lecturer at Glasgow University. During this period he developed his teaching skills and his prodigious work rate can be judged by the fact that he also completed nine chapters in one volume of what would become a classic chemistry text.^[9] In 1954, Raphael moved to Queen's University, Belfast as its first Professor of Organic Chemistry. There he published an important book on acetylene chemistry, building on his broad experience of these compounds.^[10] In 1957, Raphael returned to the University of Glasgow as the Regius Professor of Chemistry,.^[11] In 1960 he finished work on a text-book for undergraduates,^[12] which was updated and re-issued several times. In 1972 Raphael became head of the Department of Organic, Inorganic and Theoretical Chemistry at Cambridge University. This post had been made vacant by the retirement, on ill-health grounds, of Lord Todd, the previous holder of the 1702 Chair in Organic Chemistry. Raphael also became a Fellow of Christ's College. On retirement in 1988 he was granted emeritus status within his college and department, reflecting his distinguished service.^[13]

Despite having a slight stammer,^[2] Professor Raphael was an inspiring lecturer who engaged his undergraduate students with up-to-date material on organic chemistry, based on his extensive knowledge of the current literature.^[1] He had an excellent sense of humour, illustrated by Dudley Williams's report^[14][15] that

"he delivered spoof lectures. One on the synthesis of catenanes began with serious chemistry and gradually — imperceptibly — became less credible; it culminated in the description of their absorption spectra in the audible region"

The output of Raphael's own work and that of his research group of postgraduate and postdoctoral students was published in over 150 peer-reviewed articles.^[6][16][17]

Raphael was funded by external grants,^[6] including those from the SERC, NRC Canada, Glaxo Smith Kline, Hoffmann-La Roche and ICI, for whom he was a retained consultant. He also consulted for Beecham Group, Chiroscience and Fisons.^[1] His consultancy and other work led to a number of patent filings.^[18]

Raphael studied many natural products, especially of the type that were biologically active and which would provide a challenge for synthesis but might be the realistic target of a single PhD student's thesis. He and his students published syntheses of 2-deoxyribose, aaptamine, aphidicolin, apiose, arachidonic acid, arcyriaflavin B, baikiain, bullatenone, chrysanthemic acid, clovene, cordycepose, cuparene, erythrulose, exaltolide, farnesiferol C, geiparvarin, gibberone, histamine, linoleic acid, linolenic acid, lipoic acid, pseudomonic acid, pyrenophorin, Queen bee acid, shikimic acid, staurosporinone, strigol, steganacin, steganone, trichodermin and virantmicin.^[13] Raphael also investigated the composition of the wax coating of plant leaves, describing the hydrocarbons of which they are composed.^[19] In another intriguing publication in Nature, Raphael collaborated with David Rubio to identify components used in the surface treatment of the wood of stringed instruments made by Stradivarius in Cremona and showed that a version of these substances could be used to improve the tone of modern instruments.^[20]

Raphael was interested in molecules of theoretical, as well as practical, interest. In 1951, co-worked and co-authored with J. W. Cook and A. I. Scott, he published the first synthesis of the quasi-aromatic compound tropolone and the thujaplicin natural products which contained this unusual ring system.^[13]: 243 His interest in acetylenes led him to study macrocyclic compounds containing this functional group, and bridged ring systems that could be derived from them.^[6] Before the first synthesis by Ralph Raphael, thujaplicins had been naturally isolated from Chamaecyparis taiwanensis by Tetsuo Nozoe in 1936 (the β-isomer; hinokitiol),^[21] and from Thuja plicata independently by Holger Erdtman in 1948 (all three isomers; α-, β- and γ-thujaplicins).^[22]

In 1958 Raphael was elected a Fellow of the Royal Society of Edinburgh. His proposers were John Monteath Robertson, James Norman Davidson, Robert Campbell Garry, and Guido Pontecorvo.^[4] In 1962 he was also elected a Fellow of the Royal Society of London; he was the Davy Medalist for the latter in 1981.^[23] He was appointed a CBE in the Honours list of June 1982.^[24] Raphael received Honorary Doctorates from his alma mater Imperial College, in 1991,^[25] Stirling University in 1982,^[26] the University of East Anglia in 1986,^[27] and Queen's University Belfast in 1989,^[28] Among his many awards and service to learned bodies were:

In 1944 Raphael married Prudence Maguerire Anne née Gaffikin, who was a professional violin and viola player. They had a son, Tony, and a daughter, Sonia. By 1998 there were two grandchildren and a great-granddaughter. Ralph Raphael was keenly interested in the visual and performing arts, becoming a member of the Scientific Advisory Committee of the National Gallery in 1986; his favourite pastime was contract bridge. Raphael died of ischaemic heart disease, in Cambridge on 27 April 1998.^{[2][13]: 253 [32]}

• Barry M. Trost; Chao-Jun Li, eds. (2014). Modern Alkyne Chemistry: Catalytic and Atom-Economic Transformations. John Wiley & Sons. ISBN 978-3-527-67791-7.
• K. C. Nicolaou; Jason S. Chen (2011). Classics in Total Synthesis III: Further Targets, Strategies, Methods. Springer. ISBN 978-3-527-32957-1.
• J. Mann (1994). Natural products: their chemistry and biological significance. Longman Scientific & Technical. ISBN 978-0-582-06009-8.