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(2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate

Base Information Edit
  • Chemical Name:(2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate
  • CAS No.:1431879-65-0
  • Molecular Formula:C52H80O8Si2
  • Molecular Weight:889.373
  • Hs Code.:
  • Mol file:1431879-65-0.mol
(2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate

Synonyms:(2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate

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Chemical Property of (2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate Edit
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Technology Process of (2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate

There total 32 articles about (2S)-2-[(2R,3R,4aR,5'R,6S,6''R,7aR)-6''[(1E)-5-[(tert-butyldiphenylsilyl)oxy]pent-1-en-1-yl]-3-methyl-3,3''4,4a,6,6'',7,7a-octahydrodispiro[furo[3,2-b]pyran-2,2'-oxolane-5',2''-pyran]-6-yl]-2-((triisopropylsilyl)oxy)ethyl pivalate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 6 steps
1: N-iodo-succinimide; silver trifluoromethanesulfonate / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
2: chromium dichloride; nickel dichloride / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere
3: N-ethyl-N,N-diisopropylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 0.08 h / 20 °C
4: (triphenylphosphine)copper(I) hydride hexamer / water; benzene / 12 h / 20 °C / Inert atmosphere
5: potassium carbonate / methanol / 0.5 h / 20 °C / Inert atmosphere
6: pyridinium p-toluenesulfonate / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
With chromium dichloride; N-iodo-succinimide; (triphenylphosphine)copper(I) hydride hexamer; silver trifluoromethanesulfonate; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; benzene;
DOI:10.1021/ol400487e
Guidance literature:
Multi-step reaction with 11 steps
1.1: N-ethyl-N,N-diisopropylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 0.08 h / 0 °C / Inert atmosphere
2.1: tin(IV) chloride / dichloromethane / 0.17 h / -78 °C / Inert atmosphere
2.2: 0.42 h / -78 °C / Inert atmosphere
3.1: dmap; pyridine / dichloromethane / 0.08 h / 20 °C / Inert atmosphere
4.1: Pd(OH)2/C; hydrogen / ethyl acetate / 0.25 h / 20 °C
5.1: tin(IV) chloride; triethylsilane / dichloromethane / 1 h / -78 - -30 °C / Inert atmosphere
6.1: N-ethyl-N,N-diisopropylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 0.08 h / 0 °C / Inert atmosphere
7.1: chromium dichloride; nickel dichloride / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere
8.1: N-ethyl-N,N-diisopropylamine; sulfur trioxide pyridine complex / dichloromethane; dimethyl sulfoxide / 0.08 h / 20 °C
9.1: (triphenylphosphine)copper(I) hydride hexamer / water; benzene / 12 h / 20 °C / Inert atmosphere
10.1: potassium carbonate / methanol / 0.5 h / 20 °C / Inert atmosphere
11.1: pyridinium p-toluenesulfonate / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
With pyridine; chromium dichloride; triethylsilane; dmap; (triphenylphosphine)copper(I) hydride hexamer; Pd(OH)2/C; hydrogen; sulfur trioxide pyridine complex; pyridinium p-toluenesulfonate; tin(IV) chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; ethyl acetate; benzene; 2.1: |Mukaiyama Aldol Addition / 6.1: |Parikh-Doering Oxidation;
DOI:10.1021/ol400487e
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