Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids-Reference-Cited by-同舟云学术

Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids

Published:2003-01 Issue:6 Volume:13 Page:269-271
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Kravchenko Angelina N.,Chegaev Konstantin Yu.,Chikunov Il’ya E.,Belyakov Pavel A.,Maksareva Elena Yu.,Lyssenko Konstantin A.,Lebedev Oleg V.,Makhova Nina N.

Publisher

Elsevier BV

Subject

General Chemistry

Reference14 articles.

1. Syntheses of Cyclic Ureas by α-Ureidoalkylation

2. Multifunctionalized Glycolurils

3. Methods of synthesis of nitrogen-containing heterocycles using ureas and related compounds

4. Glycoluril derivatives form hydrogen bonded tapes rather than cucurbit[n]uril congeners

5. Chiral glycouril, 2,6-diethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione: spontaneous resolution, reactivity and absolute configuration

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