belactosin-c and glyoxamide

belactosin-c has been researched along with glyoxamide* in 1 studies

Other Studies

1 other study(ies) available for belactosin-c and glyoxamide

Article	Year
Total synthesis of (-)-belactosin C and derivatives via double diastereoselective tandem mukaiyama aldol lactonizations. Organic letters, 2007, Apr-12, Volume: 9, Issue:8 [reaction: see text] The enantioselective synthesis of (-)-belactosin C and derivatives was accomplished in a concise manner employing the tandem, Mukaiyama aldol-lactonizaton (TMAL) process. One approach involved a distal double diastereoselective TMAL reaction with a dipeptide glyoxamide, whereas a second approach involved amide coupling of a dipeptide with a beta-lactone carboxylic acid, obtained via the TMAL process employing a chiral silyl ketene acetal. Notable improvements in diastereoselectivity were achieved in a proximal double diastereoselective TMAL process. Topics: Acetals; Aldehydes; Dipeptides; Ketones; Lactones; Molecular Structure; Peptides; Stereoisomerism; Sulfonylurea Compounds	2007

Article

Year

Total synthesis of (-)-belactosin C and derivatives via double diastereoselective tandem mukaiyama aldol lactonizations.

Organic letters, 2007, Apr-12, Volume: 9, Issue:8

[reaction: see text] The enantioselective synthesis of (-)-belactosin C and derivatives was accomplished in a concise manner employing the tandem, Mukaiyama aldol-lactonizaton (TMAL) process. One approach involved a distal double diastereoselective TMAL reaction with a dipeptide glyoxamide, whereas a second approach involved amide coupling of a dipeptide with a beta-lactone carboxylic acid, obtained via the TMAL process employing a chiral silyl ketene acetal. Notable improvements in diastereoselectivity were achieved in a proximal double diastereoselective TMAL process.

Topics: Acetals; Aldehydes; Dipeptides; Ketones; Lactones; Molecular Structure; Peptides; Stereoisomerism; Sulfonylurea Compounds

2007