cas 145513-91-3, 1H-Indole-2-carboxylicacid,octahydro-,[2R-(2-alpha-,3a-alpha-,7a-alpha-)]-(9CI) | Articles data ｜lookchem

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145513-91-3

Articles about 145513-91-3Total 4 be found

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Efficient access to N-protected derivatives of (R,R,R)- and (S,S,S)-octahydroindole-2-carboxylic acid by HPLC resolution
The preparation of the proline analogue (2S,3aS,7aS)-octahydroindole-2-carboxylic acid (Oic) and its enantiomer, (2R,3aR,7aR)-Oic, is described. A racemic precursor has been synthesized in good yield and subjected to HPLC resolution on a chiral column. The high efficiency of both the synthetic and chromatographic procedures has allowed the isolation of multigram quantities of each amino acid in enantiomerically pure form and suitably protected for use in peptide synthesis.
Sayago, Francisco J.,Jimenez, Ana I.,Cativiela, Carlos
p. 2358 - 2364
(2008/02/12)

Synthesis and structure-activity relationships of potent new angiotensin converting enzyme inhibitors containing saturated bicyclic amino acids
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Blankley,Kaltenbronn,DeJohn,Werner,Bennett,Bobowski,Krolls,Johnson,Pearlman,Hoefle
p. 992 - 998
(2007/10/02)

DIASTEREOSELECTIVE SYNTHESIS OF BICYCLIC AMINO ACIDS VIA RING CONTRACTION OF α-CHLOROLACTAMS
Bicyclic lactams were converted to their α-chloro-derivatives and subjected to ring contraction under basic conditions to give bicyclic acids in diasteroselective fashion.
Henning, R.,Urbach, H.
p. 5339 - 5342
(2007/10/02)

COUPLING OF β-ACETAMIDO RADICALS WITH α-CHLORO ACRYLONITRILE - A NEW ACCESS TO DISUBSTITUTED PROLINE DERIVATIVES
β-Acetamido radicals are prepared by reduction of organomercurials and coupled with α-chloro-acrylonitrile.The coupling products are further converted to proline derivatives.
Henning, R.,Urbach, H.
p. 5343 - 5346
(2007/10/02)

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Chemical Properties

Boiling Point: 318.6±25.0 °C(Predicted)
Density: 1.135
Storage Temp.:Keep in dark place,Sealed in dry,Room Temperature
PKA: 2.47±0.20(Predicted)
PSA: 49.33000
LogP: 1.32050

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