cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate

cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate

The title compound, C16H20N2O2, was synthesized from (S)-tryptophan methyl ester hydrochloride and butyraldehyde. The absolute configuration 9S,10S was assigned on the basis of the unchanging chirality of the C9 centre. The NH group of the indole ring is involved in intermolecular N—H...O...

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Main Authors: Naeema Khan, Andreas Fischer, Sadaf Saeed, Mashooda Hasan, Samina Alam
Format: Article
Language:English
Published: International Union of Crystallography 2008-02-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536807066020
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spelling doaj-83dd699310e44a1c868a897bf15389e22020-11-24T20:48:53ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-02-01642o361o36110.1107/S1600536807066020cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylateNaeema KhanAndreas FischerSadaf SaeedMashooda HasanSamina AlamThe title compound, C16H20N2O2, was synthesized from (S)-tryptophan methyl ester hydrochloride and butyraldehyde. The absolute configuration 9S,10S was assigned on the basis of the unchanging chirality of the C9 centre. The NH group of the indole ring is involved in intermolecular N—H...O hydrogen bonding, while the NH group of the six-membered ring is not. This latter ring has a half-chair conformation.http://scripts.iucr.org/cgi-bin/paper?S1600536807066020
collection DOAJ
language English
format Article
sources DOAJ
author Naeema Khan
Andreas Fischer
Sadaf Saeed
Mashooda Hasan
Samina Alam
spellingShingle Naeema Khan
Andreas Fischer
Sadaf Saeed
Mashooda Hasan
Samina Alam
cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
Acta Crystallographica Section E
author_facet Naeema Khan
Andreas Fischer
Sadaf Saeed
Mashooda Hasan
Samina Alam
author_sort Naeema Khan
title cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
title_short cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
title_full cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
title_fullStr cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
title_full_unstemmed cis-(9S,10S)-Methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
title_sort cis-(9s,10s)-methyl 1-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2008-02-01
description The title compound, C16H20N2O2, was synthesized from (S)-tryptophan methyl ester hydrochloride and butyraldehyde. The absolute configuration 9S,10S was assigned on the basis of the unchanging chirality of the C9 centre. The NH group of the indole ring is involved in intermolecular N—H...O hydrogen bonding, while the NH group of the six-membered ring is not. This latter ring has a half-chair conformation.
url http://scripts.iucr.org/cgi-bin/paper?S1600536807066020
work_keys_str_mv AT naeemakhan cis9s10smethyl1propyl1234tetrahydro946carboline3carboxylate
AT andreasfischer cis9s10smethyl1propyl1234tetrahydro946carboline3carboxylate
AT sadafsaeed cis9s10smethyl1propyl1234tetrahydro946carboline3carboxylate
AT mashoodahasan cis9s10smethyl1propyl1234tetrahydro946carboline3carboxylate
AT saminaalam cis9s10smethyl1propyl1234tetrahydro946carboline3carboxylate
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