Hydromagnesiation of 3-trimethylsilyl-2-propyn-l-01 (&) followed by reaction with aldehydes or ketones affords (E)-3-trimethylsilyl-2-alken-1,4-diols (&), which can be readily dehydrated to 3-trimethylsilyl-2,5-dihydrofurans (3) by treatment with BF30Et2. The compounds 3\_ are converted to furans (5
The relative configurations of the diastbreombrs of the dl-3-amino-2-methylbutyric acid; a convenient method for their preparation via the Hofmann rearrangement
β Scribed by Ivan G. Pojarlieff; Bogdan I. Kurtev
- Book ID
- 104241859
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 138 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
11: a .jrevious i >a':'-'??" the syz.t!xoi.o of 3-anino-2-inethylbutyric acid by the Rodiozow reactioc 2 from acetaldehyde-amonia and :Ilctilyl:.lalo;lic acid *;]a0 reported. 'Tno diastareonors witi; m.p. 227-223" dcc. aid 213-214" dot. were isolated and several of their dorivativcs obtaii?ed. Ix order to establish the relative confi c;ratic-f:s of the two asymmetric carbon atom of the two axi:xo acid diaatereomrs we used the I:ofrmr~ii rearrangenc!t nhicl: ha0 bee'.: :>roved3 to proceed wit:; reteiztioa of the cc-figuratio?; of t;le carbon, atorn attac?;ed to tile a&de Croup. ior t:iis purpose we prepared the ixide of oL-2,3-dix~ethylsuccinic acid (I) a!:d the i.!O:iOtV.lidC Of %3f30-2,~-di.net~:ykiUcci~ic acid (II). zho configuration of these corqounds ha0 been carefully 1 13.1. iiurtev and I. Pojarlioff, Coinotns rerdua, Acad. bulg. sc.
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## A New Method for the Synthesis of 2,3-Aziridino-2,3dideoxyhexonamides and Their Conversion into 3-Amino-2,3dideoxyhexenoic Acids. -New 2,3-aziridino-2,3-dideoxyhexonamides (VII) and (IX) can be prepared from the lactones (I) and (VIII) via treatment of the mesylates with aqueous ammonia. The d