tedanolide and 3-hydroxybutanal

tedanolide has been researched along with 3-hydroxybutanal* in 2 studies

Other Studies

2 other study(ies) available for tedanolide and 3-hydroxybutanal

Article	Year
Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach. Organic letters, 2007, Aug-30, Volume: 9, Issue:18 The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C1-C12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1. Topics: Aldehydes; Animals; Antineoplastic Agents; Lactones; Macrolides; Molecular Structure; Porifera; Stereoisomerism	2007
Studies on the synthesis of tedanolide: synthesis of the C(5)-C(21) segment via a highly stereoselective fragment assembly aldol reaction of a chiral beta,gamma-unsaturated methyl ketone. Organic letters, 1999, Jul-15, Volume: 1, Issue:1 [formula: see text] A highly diastereoselective synthesis of 3, corresponding to the C(5)-C(21) segment of tedanolide, has been accomplished by a route utilizing the aldol reaction of aldehyde 4 and the beta,gamma-unsaturated methyl ketone 5. Topics: Aldehydes; Animals; Anti-Bacterial Agents; Antibiotics, Antineoplastic; Lactones; Macrolides; Molecular Conformation; Peptide Fragments; Porifera; Stereoisomerism	1999

Article

Year

Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach.

Organic letters, 2007, Aug-30, Volume: 9, Issue:18

The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C1-C12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1.

Topics: Aldehydes; Animals; Antineoplastic Agents; Lactones; Macrolides; Molecular Structure; Porifera; Stereoisomerism

2007

Studies on the synthesis of tedanolide: synthesis of the C(5)-C(21) segment via a highly stereoselective fragment assembly aldol reaction of a chiral beta,gamma-unsaturated methyl ketone.

Organic letters, 1999, Jul-15, Volume: 1, Issue:1

[formula: see text] A highly diastereoselective synthesis of 3, corresponding to the C(5)-C(21) segment of tedanolide, has been accomplished by a route utilizing the aldol reaction of aldehyde 4 and the beta,gamma-unsaturated methyl ketone 5.

Topics: Aldehydes; Animals; Anti-Bacterial Agents; Antibiotics, Antineoplastic; Lactones; Macrolides; Molecular Conformation; Peptide Fragments; Porifera; Stereoisomerism

1999