120205-56-3

Upstream product

• 120205-55-2 N-Z-N-Me-(S,R)-isoleucinol 
• 319-78-8 isoleucine 
• 501-53-1 benzyl chloroformate 
• 120205-55-2 benzyl [(2S,3S)-1-hydroxy-3-methylpentan-2-yl]methylcarbamate 
• 42417-66-3 (2S,3S)-3-methyl-2-(methyl{[(phenylmethyl)oxy]carbonyl}amino)pentanoic acid 
• 163887-30-7 N-Z-N-Me-(S,R)-Ile 
• 3160-59-6 N-benzyloxycarbonyl-isoleucine 
• 3160-59-6 N-Cbz-L-Isoleucine 

Downstream Products

• 120205-57-4 tert-butyl 3-hydroxy-4(S)-(N-Z-N-Me)-5(R)-methylheptanoate 
• 120205-57-4 tert-Butyl (3S,4S,5S)-3-hydroxy-4--5-methylheptanoate 
• 120294-43-1 tert-Butyl (3R,4S,5S)-3-hydroxy-4--5-methylheptanoate 
• 177659-48-2 [(1S,2R,3S)-1-((S)-sec-Butyl)-2-hydroxy-4-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-3-methylsulfanyl-4-oxo-butyl]-methyl-carbamic acid benzyl ester 
• 177659-46-0 [(1S,2R)-1-((S)-sec-Butyl)-2-hydroxy-4-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-4-oxo-butyl]-methyl-carbamic acid benzyl ester 
• 716371-48-1 (1R)-2-endo-[(3R,4S,5S)-4-(N-benzyloxycarbonyl-N-methylamino)-3-hydroxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 716371-64-1 (3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoic acid 
• 716371-60-7 (1R)-2-endo-[(3R,4S,5S)-4-(N-benzyloxycarbonyl-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 716371-62-9 (1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 716371-63-0 (1R)-2-endo-[(3R,4S,5S)-4-(N-((2S)-((2S)-N-benzyloxycarbonylamino-3-methylbutanoyl)-3-methylbutanoyl)-N-methylamino)-3-methoxy-5-methylheptanoyl]-2-exo-trimethylsilyloxy-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 110417-88-4 dolastatin 10 
• 154633-73-5 tert-Butyl (3S,4S,5S)-3-methoxy-4--5-methylheptanoate 
• 120205-48-3 tert-Butyl (3R,4S,5S)-3-methoxy-4-(N-methylamino)-5-methylheptanoate hydrochloride 
• 120205-53-0 (3R,4S,5S)-tert-butyl 4-((S)-2-((S)-2-(dimethylamino)-3-methylbutanamido)-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoate 

Relevant academic research and scientific papers

CYTOTOXIC PEPTIDES AND ANTIBODY DRUG CONJUGATES THEREOF

The present invention is directed to cytotoxic pentapeptides, to antibody drug conjugates thereof, and to methods for using the same to treat cancer.

A practical total synthesis of hapalosin, a 12-membered cyclic depsipeptide with multidrug resistance-reversing activity, by employing improved segment coupling and macrolactonization

A practical total synthesis of hapalosin, a compound with multidrug resistance-reversing activity, has been carried out using an unprecedented macrolactonization strategy. One of the features of the new approach is the straightforward and fully stereocont

The dolastatins. 19. Synthesis of dolaisoleuine

The synthesis of dolaisoleuine as its tert-butyl ester (Dil-OBu(t)), a β- methoxy-γ-amino acid component of dolastatin 10, has been achieved employing as key step an aldol condensation between N-(benzyloxycarbonyl)-N-methyl- (S,S)-isoleucinal and tert-butyl acetate followed by O-methylation. The overall six-step reaction sequence to Dil proved to be convenient for routine preparation of this new amino acid and its stereochemical assignment as (3R,4S,5S)-N,O-dimethylisostatine.