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Aggarwal

I. D. Aggarwal, S. Earquharson, and E. Koglin, eds.. Proceedings of SPIE—The International Societyfor Optical Engineering 2561, 243p (1995). [Pg.295]

Harrison, S.C., Aggarwal, A.K. DNA recognition by proteins with the helix-tum-helix motif. Anna. Rev. Biochem. 59 933-969, 1990. [Pg.148]

Varinder K. Aggarwal Synthetic Chemistry School of Chemistry Cantock s Close Bristol BS8 ITS UK... [Pg.1]

Varinder K. Aggarwal, D. Michael Badine, and Vijayalakshmi A Moorthie... [Pg.3]

The Aggarwal group has used chiral sulfide 7, derived from camphorsulfonyl chloride, in asymmetric epoxidation [4]. Firstly, they prefonned the salt 8 from either the bromide or the alcohol, and then formed the ylide in the presence of a range of carbonyl compounds. This process proved effective for the synthesis of aryl-aryl, aryl-heteroaryl, aryl-alkyl, and aryl-vinyl epoxides (Table 1.2, Entries 1-5). [Pg.4]

One class of particularly challenging targets for asymmetric epoxidation is that of terminal epoxides. Aggarwal and co-workers found that zinc carbenoids generated... [Pg.12]

Of course, the key limitation of the ylide-mediated methods discussed so far is the use of stoichiometric amounts of the chiral reagent. Building on their success with catalytic asymmetric ylide-mediated epoxidation (see Section 1.2.1.2), Aggarwal and co-workers have reported an aza version that provides a highly efficient catalytic asymmetric synthesis of trans-aziridines from imines and diazo compounds or the corresponding tosylhydrazone salts (Scheme 1.43) [68-70]. [Pg.33]


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See also in sourсe #XX -- [ Pg.110 , Pg.184 , Pg.395 , Pg.396 , Pg.400 , Pg.404 , Pg.405 , Pg.406 ]

See also in sourсe #XX -- [ Pg.435 ]




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