901121-97-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 901121-92-4 C₂₃H₃₄N₂O₃ 
• 901121-80-0 (2E,8Z,10E)-12-(tert-butyl-dimethyl-silanyloxy)-9-(2-oxo-oxazolidin-3-yl)-trideca-2,8,10,12-tetraen-1-al 
• 901121-79-7 3-{(1Z)-1-[(Z)-3-(tert-butyl-dimethyl-silanyloxy)-but-1,3-dienyl]-octa-1,7-dienyl}-oxazolidin-2-one 
• 901121-78-6 (+/-)-3-{(1Z)-1-[(E)-(3-tert-butyl-dimethyl-silanyloxy)-but-1-enyl]-octa-1,7-dienyl}-oxazolidin-2-one 
• 901121-86-6 (+/-)-3-[(1Z)-1-((E)-3-oxo-but-1-enyl)-octa-1,7-dienyl]-oxazolidin-2-one 
• 901121-85-5 (+/-)-3-[(1Z)-1-((E)-3-hydroxy-but-1-enyl)-octa-1,7-dienyl]-oxazolidin-2-one 
• 901121-77-5 (+/-)-(2E,4Z)-(4-bromo-1-methyl-undeca-2,4,10-trienyloxy)-tert-butyl-dimethyl-silane 
• 901121-88-8 (-)-(R)-(1-methyl-5-oxo-hexyl)-carbamic acid tert-butyl ester 
• 929119-04-0 C₂₈H₃₇NO₄ 
• 901121-94-6 C₃₁H₄₀N₂O₅ 

Downstream Products

• 16625-34-6 (+)-galbulimima alkaloid 13 

Relevant academic research and scientific papers

Total synthesis of (+)-galbulimima alkaloid 13 and (+)-himgaline

The stereoselective syntheses of (+)-himgaline (1) and (+)-GB13 (2) are described. Important diastereoselective bond constructions include an intramolecular Diels-Alder reaction, an intramolecular Michael addition, and an intramolecular enamine aldol addi

Total synthesis and absolute stereochemical assignment of (+)- and (-)-galbulimima alkaloid 13

We describe the total synthesis of (+)- and (-)-galbulimima alkaloid 13. The absolute stereochemistry of natural (-)-galbulimima alkaloid 13 is revised to 2S. Sequential use of catalytic cross-coupling and cross-metathesis reactions followed by an intramo