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1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S,4S)-

Base Information
  • Chemical Name:1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S,4S)-
  • CAS No.:403503-40-2
  • Molecular Formula:C16H19NO6
  • Molecular Weight:321.33
  • Hs Code.:
1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl
1-(phenylmethyl) ester, (2S,4S)-

Synonyms:

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Chemical Property of 1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S,4S)-
Chemical Property:
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Technology Process of 1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S,4S)-

There total 6 articles about 1,2-Piperidinedicarboxylic acid, 4-(formyloxy)-, 2-methyl 1-(phenylmethyl) ester, (2S,4S)- 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:
4-formyloxy-(S)-pipecolic acid methyl ester; With tert-butyl methyl ether; lipase AY30 (Candida rugosa, Amano); In aq. phosphate buffer; at 20 ℃; for 96h; pH=7; Resolution of racemate; Enzymatic reaction;
phthalic anhydride; With dmap; triethylamine; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/op020017x
Guidance literature:
With triphenylphosphine; diethylazodicarboxylate; Multistep reaction; 1.) THF, 1 h, 2.) THF, RT, overnight;
DOI:10.1016/S0960-894X(98)00231-5
Guidance literature:
Multi-step reaction with 2 steps
1.1: H2; HCl / Pd(OH)2/C / methanol
1.2: 84 percent / Na2CO3 / 0 °C
2.1: DEAD; Ph3P / tetrahydrofuran / 5 °C
With hydrogenchloride; hydrogen; triphenylphosphine; diethylazodicarboxylate; palladium dihydroxide; In tetrahydrofuran; methanol; 2.1: Mitsunobu inversion;
DOI:10.1016/S0040-4039(01)01660-4
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