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In natural product chemistry

Fourteen syntheses of cis-jasmone are given in chart from in Natural Products Chemistry ed. K.Nakanishi et. ah. Academic Press, New York, 1975, vol.2, p.21. [Pg.136]

Synthetic utility of stereoselective alkylations in natural product chemistry is exemplified by the preparation of optically active 2-arylglycine esters (38). Chirally specific a-amino acids with methoxyaryl groups attached to the a-carbon were prepared by reaction of the dimethyl ether of a chiral bis-lactam derivative with methoxy arenes. Using SnCl as the Lewis acid, enantioselectivities ranging from 65 to 95% were obtained. [Pg.553]

Epoxide-opening iatramolecular cycli2ations, in light of their importance in natural product chemistry, have received much attention (62). [Pg.555]

G. Gribble and S. Berthel, Studies in Natural Products Chemistry, Vol. 12. Elsevier Science Publishers, New York, 1993. [Pg.153]

Heterocyclic Mesomeric Betaines and Analogs in Natural Product Chemistry. Betainic Alkaloids and Nucleobases... [Pg.67]

It is my opinion that this approach has considerable merit, provided that the questions posed in the problems are wisely selected, as indeed they are in this text. The authors themselves are well versed in natural-product chemistry, an area that presents a wide array of small molecule structural problems. They are therefore concerned that the reader reach the practical goal of applying the full power of NMR spectroscopy to problems of this type. To this end they have selected problems that address methods for solving structures as well as those that pertain to basic theory. The authors have wisely made a point of treating the more widely used ID and 2D experiments in considerable detail. Nevertheless, they also introduce the reader to many of the less common techniques. [Pg.435]

Scheme 2. Reprinted with permission from I. Fleming in New Trends in Natural Products Chemistry 1986 (A. U. Rahman and P. W. Le Quesne, eds), p. 84, 89-92, Pergamon Books Limited, 1986. Scheme 2. Reprinted with permission from I. Fleming in New Trends in Natural Products Chemistry 1986 (A. U. Rahman and P. W. Le Quesne, eds), p. 84, 89-92, Pergamon Books Limited, 1986.
Ballini, R. Studies in Natural Products Chemistry, ed. by A. Rahman, Elsevier, Amsterdam, 19, 117 (1997). [Pg.124]

Braekman JC, Daloze D (1990) Chemical defense in ants. In Atta-ur-Rahman (ed) Studies in natural products chemistry, vol 6. Stereoselective synthesis (Part D). Elsevier, Amsterdam, p 421... [Pg.238]

Ulubelen, A., Meri9li, A. H. and Meri9li, F., 1998, Advances in Natural Product Chemistry (Ed. Atth-ur-Rahman, M. I. Choudhary, Harwood, Academic Publishers, USA, pp 247-260. [Pg.54]

Atta-ur-Rahman and Choudhary, M.I., 1988, Structural studies on new steroidal alkaloids of Buxus papillosa. In Studies in Natural Products Chemistry (Atta-ur-Rahman ed.), Elsevier Science, Amsterdam, Vol. 2, pp 175-189. [Pg.65]

Here, we will present a selection of the most attractive naturally occurring phenazines that have been newly discovered. Also, we will deal with the general methods of phenazine synthesis and its most recent applications in natural product chemistry. Until now, the relevance of Pd-catalyzed N-arylations to this... [Pg.79]

New Trends in Natural Products Chemistry 1986 edited by Atta-ur-Rahman and P.W. Le Quesne... [Pg.546]

Gaffield, W. (2000). The Veratrum alkaloids Natural tools for studying embryonic development, in Atta-ur-Rahman, Ed., Studies in natural products chemistry 23, Elsevier Science, Amsterdam, pp. 563-589. [Pg.66]

The environmentally benign synthesis of lactones has attracted attention because of their importance in natural product chemistry. The oxidative cyclization of diols via carbon-oxygen bond formation is the most well-known approach for the synthesis of lactones [70]. [Pg.135]

Kubo I, Nakatsu T (1990) Recent Examples of Preparative-Scale Recycling High Performance Liquid Chromatography in Natural Products Chemistry. LC-GC 8 933... [Pg.152]

The novel horizons in natural product chemistry are a consequence of advances in mass spectrometry instrumentation. Current applications comprise the elucidation of natural products as part of total extract mixtures in samples of interest to environmental chemists, archaelogists, paleobotanists, geologists, oceanographers, atmospheric chemists, forensic chemists and engineers. The list of applications is expected to expand and some examples are discussed in this chapter. [Pg.79]

J. Bergman, in "Studies in Natural Product Chemistry Stereoselective Sjmthesis (Part A)" ( Atta-ur-Rahman, ed.), vol. 1, p. 3. Elsevier, Amsterdam, 1988. [Pg.396]

Lundt I (2003) Iminosugars, isoiminosugars, and carbasugars from activated carbohydrate lactones efficient synthesis of biologically important compounds. In Witzak ZJ, Tatsuta K (eds) Carbohydrate synthons in natural products chemistry synthesis, functionalization and applications. ACS Symposium Series, vol 841. American Chemical Society, Washington, DC,pp 117-140... [Pg.56]


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See also in sourсe #XX -- [ Pg.707 , Pg.708 , Pg.717 , Pg.718 , Pg.719 ]




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