136262-53-8

Upstream product

• 143-33-9 sodium cyanide 
• 186642-08-0 (R)-1-bromo-3-(tert-butyldiphenylsilyloxy)-2-methylpropane 
• 773837-37-9 sodium cyanide 
• 136786-35-1 (2R)-3-(tert-butyldiphenylsilyloxy)-2-methylpropyl p-toluenesulfonate 
• 95514-04-8 (S)-3-(tert-butyldiphenylsilyloxy)-2-methylpropan-1-ol 
• 95514-03-7 (R)-methyl 3-(tert-butyl(diphenyl)silyloxy)-2-methylpropanoate 
• 151-50-8 potassium cyanide 
• 123444-67-7 (R)-3-[(tert-butyl)diphenylsilyloxy]-1-iodo-2-methylpropane 
• 136292-93-8 Methanesulfonic acid (R)-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propyl ester 

Downstream Products

• 123444-68-8 (S)-4-(tert-butyldiphenylsilyloxy)-3-methylbutanal 
• 887278-78-6 tert-butyl-((2S,6S)-2,6-dimethyltridecyloxy)-diphenyl silane 
• 123444-69-9 (2S)-tert-butyl(2-methylpent-4-ynyloxy)diphenylsilane 
• 123465-13-4 (E)-(3S,7S,8S)-2-Benzenesulfonyl-8,9-bis-benzyloxy-7-benzyloxymethyl-1-[(2S,3S,5R,6S)-3-(tert-butyl-dimethyl-silanyloxy)-6-methoxy-5-methyl-tetrahydro-pyran-2-yl]-3,5-dimethyl-non-5-en-1-one 
• 123444-72-4 (E)-(3S,7S,8S)-8,9-Bis-benzyloxy-7-benzyloxymethyl-1-[(2S,3S,5R,6S)-3-(tert-butyl-dimethyl-silanyloxy)-6-methoxy-5-methyl-tetrahydro-pyran-2-yl]-3,5-dimethyl-non-5-en-1-one 
• 123444-73-5 (E)-(3S,7S,8S)-8,9-Bis-benzyloxy-7-benzyloxymethyl-1-((2S,3S,5R,6S)-3-hydroxy-6-methoxy-5-methyl-tetrahydro-pyran-2-yl)-3,5-dimethyl-non-5-en-1-one 
• 123444-74-6 (2R,3S,5R,6S)-2-((E)-(1S,3S,7S,8S)-8,9-Bis-benzyloxy-7-benzyloxymethyl-1-methoxy-3,5-dimethyl-non-5-enyl)-3,6-dimethoxy-5-methyl-tetrahydro-pyran 
• 123444-70-2 (E)-(2S,3S,7S)-1-Benzyloxy-3-benzyloxymethyl-8-(tert-butyl-diphenyl-silanyloxy)-5,7-dimethyl-oct-4-en-2-ol 
• 123444-71-3 C₃₈H₄₄O₅S 
• 136262-69-6 tert-Butyl-[(E)-(2S,4S,5R,6S)-4,5-dimethoxy-2,6-dimethyl-8-((4R,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-non-7-enyloxy]-diphenyl-silane 
• 136374-56-6 tert-Butyl-[(E)-(2S,4S,5R,6R)-4,5-dimethoxy-2,6-dimethyl-8-((4R,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-non-7-enyloxy]-diphenyl-silane 

Relevant academic research and scientific papers

3,6-DIAMINO-PYRIDAZIN-3-YL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR USES AS PRO-APOPTOTIC AGENTS

Compounds of formula (I) wherein Het1, Het2, R1, R2 and R3 are as defined in the description. Medicaments.

Synthesis of stereopure acyclic 1,5-dimethylalkane chirons: Building blocks of highly methyl-branched natural products

An efficient synthetic method towards stereopure acyclic 1,5-dimethylalkane building blocks from methyl (2R)-3-hydroxy-2-methylpropionate (R)-1 (>99% ee) and methyl (2S)-3-hydroxy-2-methylpropionate (S)-1 (>99% ee) through a series of chemical transformat

Anti-AIDS agents 81. design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors

In our continuing study of triterpene derivatives as potent anti-HIV agents, different C-3 conformationally restricted betulinic acid (BA, 1) derivatives were designed and synthesized in order to explore the conformational space of the C-3 pharmacophore. 3-O-Monomethylsuccinyl-betulinic acid (MSB) analogues were also designed to better understand the contribution of the C-3′ dimethyl group of bevirimat (2), the first-in-class HIV maturation inhibitor, which is currently in phase IIb clinical trials. In addition, another triterpene skeleton, moronic acid (MA, 3), was also employed to study the influence of the backbone and the C-3 modification toward the anti-HIV activity of this compound class. This study enabled us to better understand the structure-activity relationships (SAR) of triterpene-derived anti-HIV agents and led to the design and synthesis of compound 12 (EC50: 0.0006 μM), which displayed slightly better activity than 2 as a HIV-1 maturation inhibitor.

Anti-AIDS agents 73: Structure-activity relationship study and asymmetric synthesis of 3-O-monomethylsuccinyl-betulinic acid derivatives

3-O-3′(or 2′)-Methylsuccinyl-betulinic acid (MSB) derivatives were separated by using recycle HPLC. The structures of four isomers were assigned by NMR and asymmetric synthesis. 3-O-3′S-Methylsuccinyl-betulinic acid (3′S-MSB, 4) exhibited potent anti-HIV

Synthesis of optically active diastereomers of a nonproteic neurotrophic mimetic

The four diastereomers 3, elongated analogues of perhydroretinol, are synthesized starting from both optically pure 3-bromo-2-methyl-1-propanol enantiomers. All exhibit neurotrophic activity on cultured neuronal cells derived from fetal rat cerebral hemispheres.

Total Synthesis of (-)-Stemoamide

An enantiocontrolled total synthesis of the tricyclic alkaloid, stemoamide (2), is reported. Key Words: Asymmetric aldol; chiral butyrolactone synthesis; selective 1,3-acyclic diol formation.

AN ENANTIOSELECTIVE SYNTHESIS OF THE C(10) TO C(23) BACKBONE OF THE POTENT IMMUNOSUPPRESSANT FK506

The C(10) to C(23) fragment of FK506 has been pepared in a convergent, highly stereocontrolled, fashion.The key transformations entailed opening of a symmetrical trans-disubstituted epoxide with a trisubstituted vinylalane ate complex, the reductive remov