Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitrogen derivatives alkylation, stereochemistry

J.l Regiochemistry and Stereochemistry of Alkylations of Nitrogen Derivatives of Carbonyl Compounds... [Pg.1]

Chiral alkoxy allenes derived from 1,3-alkylidene-L-erythritol and -D-threitol have been used in cycloaddition reactions to provide the 4-substituted /3-lactams 418 (R = Me, Ph). Intramolecular alkylation at nitrogen was achieved by the action of potassium carbonate and tetrabutylammonium bromide in dry acetonitrile. The absolute stereochemistry of the product 419 (R = Me, Ph) was assigned on the basis of the CD helicity rule (see Section 2.04.3.5) and NMR spectroscopy. The [2+2] cycloaddition of CSI to threitol vinyl ethers was found to have low stereoselectivity in contrast to the findings with erythritol derivatives <2004CH414, 2005EJ0429>. [Pg.296]

Several V- IJ<>c-A-MOM-a-am ino acid derivatives undergo a-methylation in 78% to nearly 93% ee with retention of the configuration upon treatment with KHMDS followed by methyl iodide at —78°C. The substituents of the nitrogen are essential for control of the stereochemistry. How much is the stereochemical course of the reaction affected by an additional chiral center at C(3) of substrates a-Alkylation of A -lioc-A-MOM-L-isoleucine derivative 61 and its C(2)-epimer, D-a/fo-isoleucine derivative 62, were investigated (Scheme 3.16). If the chirality at C(2) is completely lost with formation of the enolate, a-methylation of either 61 or 62 should give a mixture of 63 and 64 with an identical diastereomeric composition via common enolate intermediate K. On the other hand, if the chirality of C(2) is memorized in enolate intermediates, 61 and 62 should give products with independent diastereomeric compositions via diastereomeric enolate intermediates. [Pg.194]

An interesting example of substrate control was also achieved in the rearrangement of ammonium salt 30 (Scheme 17.8). As part of a program to develop novel antibiotics, it was of interest to alkylate the C3 position of the lactam ring in penicillin derivatives while maintaining the cis stereochemistry between the nitrogen and sulfur moieties. Toward this end, amine 29, which is available from A7,A7-dimethylaminopenicillanic acid hydrochloride, was quatemized with allyl bromide to afford compound 30. When this material was treated with sodium hydride at... [Pg.479]


See other pages where Nitrogen derivatives alkylation, stereochemistry is mentioned: [Pg.223]    [Pg.955]    [Pg.997]    [Pg.112]    [Pg.129]    [Pg.129]    [Pg.1006]    [Pg.265]    [Pg.153]    [Pg.56]    [Pg.31]    [Pg.169]    [Pg.86]    [Pg.51]    [Pg.1953]    [Pg.378]    [Pg.404]    [Pg.55]    [Pg.181]    [Pg.361]    [Pg.503]    [Pg.503]    [Pg.120]    [Pg.91]    [Pg.29]    [Pg.181]    [Pg.112]    [Pg.730]    [Pg.37]    [Pg.93]    [Pg.149]    [Pg.154]    [Pg.147]    [Pg.201]    [Pg.306]    [Pg.13]    [Pg.503]   
See also in sourсe #XX -- [ Pg.3 , Pg.28 ]




SEARCH



Alkyl derivatives

Alkylation nitrogen

Alkylation stereochemistry

Nitrogen derivatives

Nitrogen stereochemistry

Nitrogenous Derivatives

© 2024 chempedia.info