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1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)-

1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)- ??? ???
?? ??:
123724-21-0
???:
1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)-
???(??):
(2S,3R)-1-Boc-3-phenylpyrrolidine-2-carboxylic Acid;(2S,3R)-1-(tert-butoxycarbonyl)-3-phenylpyrrolidine-2-carboxylic acid;(2S,3R)-1-tert-butoxycarbonyl-3-phenyl-pyrrolidine-2-carboxylic acid - [B81879];1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)-;(2S,3R)-1-[(2-Methylpropan-2-YL)oxycarbonyl]-3-phenylpyrrolidine-2-carboxylic acid
CBNumber:
CB55484563
???:
C16H21NO4
??? ??:
291.34
MOL ??:
123724-21-0.mol

1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)- ??

???
161-162 °C
?? ?
441.5±45.0 °C(Predicted)
??
1.196±0.06 g/cm3(Predicted)
?? ?? (pKa)
3.85±0.40(Predicted)

??

1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)- C??? ??, ??, ??

??

(3R)-Phenylpyrrolidine-1,(2S)-dicarboxylic Acid 1-tert-butyl Ester is used in the synthesis of 3-substituted pyroglutamic acids and prolines via asymmetric Michael addition reactions between Ni(II)-complexes of glycine Schiff bases and chiral (alkenoyl)(phenyl)oxazolidinones.

1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)- ?? ?? ? ???

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1,2-Pyrrolidinedicarboxylic acid, 3-phenyl-, 1-(1,1-dimethylethyl) ester, (2S,3R)- ?? ??

???( 13)?? ??
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