Design, Synthesis, and Evaluation of Carbamate-Substituted Analogues of (+)-Discodermolide
摘要:
The design, syntheses, and biological evaluation of 22 totally synthetic analogues of the potent microtubule-stabilizing agent (divided by)-discodermolide (1) have been achieved. Structure-activity relationships of the C(19) carbamate were defined. exploiting two synthetically simplified scaffolds. as well as the parent (+)-discodermolide framework.
Design, Synthesis, and Evaluation of Analogues of (+)-14-Normethyldiscodermolide
摘要:
The design, syntheses, and biological evaluation of nine totally synthetic analogues of the microtubule-stabilizing agent (divided by)-14-normethyldiscodermolide (2) are reported. Simplification at the C(21)-C(24) terminal diene and at the C(1)-C(5) lactone moieties reveals significant structure-activity relationships.
Design, Synthesis, and Evaluation of Analogues of (+)-14-Normethyldiscodermolide
作者:Amos B. Smith、B. Scott Freeze、Matthew J. LaMarche、Tomoyasu Hirose、Ignacio Brouard、Ming Xian、Kurt F. Sundermann、Simon J. Shaw、Mark A. Burlingame、Susan Band Horwitz、David C. Myles
DOI:10.1021/ol0476873
日期:2005.1.1
The design, syntheses, and biological evaluation of nine totally synthetic analogues of the microtubule-stabilizing agent (divided by)-14-normethyldiscodermolide (2) are reported. Simplification at the C(21)-C(24) terminal diene and at the C(1)-C(5) lactone moieties reveals significant structure-activity relationships.
Design, Synthesis, and Evaluation of Carbamate-Substituted Analogues of (+)-Discodermolide
作者:Amos B. Smith、B. Scott Freeze、Matthew J. LaMarche、Tomoyasu Hirose、Ignacio Brouard、Paul V. Rucker、Ming Xian、Kurt F. Sundermann、Simon J. Shaw、Mark A. Burlingame、Susan Band Horwitz、David C. Myles
DOI:10.1021/ol047686a
日期:2005.1.1
The design, syntheses, and biological evaluation of 22 totally synthetic analogues of the potent microtubule-stabilizing agent (divided by)-discodermolide (1) have been achieved. Structure-activity relationships of the C(19) carbamate were defined. exploiting two synthetically simplified scaffolds. as well as the parent (+)-discodermolide framework.