skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 63  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 next page
Show only
Refined by: subject: Chemistry remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
Material Type:
Article 		Add to My Research

The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters

Accounts of chemical research, 2004-08, Vol.37 (8), p.506-517 [Peer Reviewed Journal]

Copyright © 2004 American Chemical Society ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/ar0300625 ;PMID: 15311949

Full text available

Citations Cited by
2
Preparation and Use of a General Solid-Phase Intermediate to Biomimetic Scaffolds and Peptide Condensations
Preparation and Use of a General Solid-Phase Intermediate to Biomimetic Scaffolds and Peptide Condensations
Material Type:
Article 		Add to My Research

Preparation and Use of a General Solid-Phase Intermediate to Biomimetic Scaffolds and Peptide Condensations

Molecules (Basel, Switzerland), 2018-07, Vol.23 (7), p.1762 [Peer Reviewed Journal]

2018. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 by the authors. 2018 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules23071762 ;PMID: 30021979

Full text available

Citations Cited by
3
Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations
Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations
Material Type:
Article 		Add to My Research

Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations

Molecules (Basel, Switzerland), 2016-03, Vol.21 (3), p.350-350 [Peer Reviewed Journal]

2016 by the authors. 2016 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules21030350 ;PMID: 26999079

Full text available

Citations Cited by
4
Catalytic Enantioselective Synthesis of Glutamic Acid Derivatives via Tandem Conjugate Addition−Elimination of Activated Allylic Acetates under Chiral PTC Conditions
Catalytic Enantioselective Synthesis of Glutamic Acid Derivatives via Tandem Conjugate Addition−Elimination of Activated Allylic Acetates under Chiral PTC Conditions
Material Type:
Article 		Add to My Research

Catalytic Enantioselective Synthesis of Glutamic Acid Derivatives via Tandem Conjugate Addition−Elimination of Activated Allylic Acetates under Chiral PTC Conditions

Journal of the American Chemical Society, 2005-10, Vol.127 (39), p.13450-13451 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja052638m ;PMID: 16190680 ;CODEN: JACSAT

Full text available

Citations Cited by
5
Solid-Phase Synthesis of Multiple Classes of Peptidomimetics from Versatile Resin-Bound Aldehyde Intermediates
Solid-Phase Synthesis of Multiple Classes of Peptidomimetics from Versatile Resin-Bound Aldehyde Intermediates
Material Type:
Article 		Add to My Research

Solid-Phase Synthesis of Multiple Classes of Peptidomimetics from Versatile Resin-Bound Aldehyde Intermediates

Journal of the American Chemical Society, 2007-06, Vol.129 (22), p.7077-7088 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja069188y ;PMID: 17503818

Full text available

Citations Cited by
6
Solid-phase synthetic route to multiple derivatives of a fundamental peptide unit
Solid-phase synthetic route to multiple derivatives of a fundamental peptide unit
Material Type:
Article 		Add to My Research

Solid-phase synthetic route to multiple derivatives of a fundamental peptide unit

Molecules (Basel, Switzerland), 2010-07, Vol.15 (7), p.4961-4983 [Peer Reviewed Journal]

Copyright MDPI AG 2010 ;2010 by the authors; 2010 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules15074961 ;PMID: 20657403

Full text available

Citations Cited by
7
Global mean potassium intake: a systematic review and Bayesian meta-analysis
Global mean potassium intake: a systematic review and Bayesian meta-analysis
Material Type:
Article 		Add to My Research

Global mean potassium intake: a systematic review and Bayesian meta-analysis

European journal of nutrition, 2023-08, Vol.62 (5), p.2027-2037 [Peer Reviewed Journal]

The Author(s) 2023 ;ISSN: 1436-6207 ;EISSN: 1436-6215 ;DOI: 10.1007/s00394-023-03128-6

Digital Resources/Online E-Resources

Citations Cited by
8
Solid-Phase Unnatural Peptide Synthesis (UPS)
Solid-Phase Unnatural Peptide Synthesis (UPS)
Material Type:
Article 		Add to My Research

Solid-Phase Unnatural Peptide Synthesis (UPS)

Journal of the American Chemical Society, 1996-06, Vol.118 (25), p.6070-6071 [Peer Reviewed Journal]

Copyright © 1996 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja9601245

Full text available

Citations Cited by
9
Acyclic Stereoselective Boron Alkylation Reactions for the Asymmetric Synthesis of β-Substituted α-Amino Acid Derivatives
Acyclic Stereoselective Boron Alkylation Reactions for the Asymmetric Synthesis of β-Substituted α-Amino Acid Derivatives
Material Type:
Article 		Add to My Research

Acyclic Stereoselective Boron Alkylation Reactions for the Asymmetric Synthesis of β-Substituted α-Amino Acid Derivatives

Journal of the American Chemical Society, 2003-03, Vol.125 (9), p.2370-2371 [Peer Reviewed Journal]

Copyright © 2003 American Chemical Society ;2003 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja0298794 ;PMID: 12603106 ;CODEN: JACSAT

Full text available

Citations Cited by
10
Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters
Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters
Material Type:
Article 		Add to My Research

Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters

Tetrahedron, 2001-07, Vol.57 (30), p.6641-6650 [Peer Reviewed Journal]

2001 Elsevier Science Ltd ;ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/S0040-4020(01)00554-3

Full text available

Citations Cited by
11
The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis
The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis
Material Type:
Article 		Add to My Research

The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis

Journal of the American Chemical Society, 1989-03, Vol.111 (6), p.2353-2355 [Peer Reviewed Journal]

1990 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja00188a089 ;CODEN: JACSAT

Full text available

Citations Cited by
12
A Solid-Phase Synthetic Route to Unnatural Amino Acids with Diverse Side-Chain Substitutions
A Solid-Phase Synthetic Route to Unnatural Amino Acids with Diverse Side-Chain Substitutions
Material Type:
Article 		Add to My Research

A Solid-Phase Synthetic Route to Unnatural Amino Acids with Diverse Side-Chain Substitutions

Journal of organic chemistry, 2002-05, Vol.67 (9), p.2960-2969 [Peer Reviewed Journal]

Copyright © 2002 American Chemical Society ;2002 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo016236i ;PMID: 11975553 ;CODEN: JOCEAH

Full text available

Citations Cited by
13
The Enantioselective Synthesis of α-Amino Acid Derivatives via Organoboranes
The Enantioselective Synthesis of α-Amino Acid Derivatives via Organoboranes
Material Type:
Article 		Add to My Research

The Enantioselective Synthesis of α-Amino Acid Derivatives via Organoboranes

Journal of the American Chemical Society, 2002-08, Vol.124 (32), p.9348-9349 [Peer Reviewed Journal]

Copyright © 2002 American Chemical Society ;2002 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja017522e ;PMID: 12167010 ;CODEN: JACSAT

Full text available

Citations Cited by
14
Theoretical studies in molecular recognition: asymmetric induction of benzophenone imine ester enolates by the benzylcinchoninium ion
Theoretical studies in molecular recognition: asymmetric induction of benzophenone imine ester enolates by the benzylcinchoninium ion
Material Type:
Article 		Add to My Research

Theoretical studies in molecular recognition: asymmetric induction of benzophenone imine ester enolates by the benzylcinchoninium ion

Journal of organic chemistry, 1991-08, Vol.56 (17), p.5181-5192 [Peer Reviewed Journal]

1992 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo00017a035 ;CODEN: JOCEAH

Full text available

Citations Cited by
15
The regioselective α-alkylation of the benzophenone imine of glycinamide, alaninamide, and related derivatives
The regioselective α-alkylation of the benzophenone imine of glycinamide, alaninamide, and related derivatives
Material Type:
Article 		Add to My Research

The regioselective α-alkylation of the benzophenone imine of glycinamide, alaninamide, and related derivatives

Canadian journal of chemistry, 2006-10, Vol.84 (10), p.1301-1312 [Peer Reviewed Journal]

COPYRIGHT 2006 NRC Research Press ;ISSN: 0008-4042 ;EISSN: 1480-3291 ;DOI: 10.1139/v06-088

Full text available

Citations Cited by
16
Solid-phase synthesis of amino amides and peptide amides with unnatural side chains
Solid-phase synthesis of amino amides and peptide amides with unnatural side chains
Material Type:
Article 		Add to My Research

Solid-phase synthesis of amino amides and peptide amides with unnatural side chains

Tetrahedron letters, 2001-03, Vol.42 (11), p.2073-2076 [Peer Reviewed Journal]

2001 Elsevier Science Ltd ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/S0040-4039(01)00090-9

Full text available

Citations Cited by
17
A new active catalyst species for enantioselective alkylation by phase-transfer catalysis
A new active catalyst species for enantioselective alkylation by phase-transfer catalysis
Material Type:
Article 		Add to My Research

A new active catalyst species for enantioselective alkylation by phase-transfer catalysis

Tetrahedron, 1994-04, Vol.50 (15), p.4507-4518 [Peer Reviewed Journal]

1994 ;ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/S0040-4020(01)89382-0

Full text available

Citations Cited by
18
Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael addition reactions
Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael addition reactions
Material Type:
Article 		Add to My Research

Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael addition reactions

Tetrahedron: asymmetry, , Vol.12 (6), p.821-828 [Peer Reviewed Journal]

2001 Elsevier Science Ltd ;ISSN: 0957-4166 ;EISSN: 1362-511X ;DOI: 10.1016/S0957-4166(01)00116-1

Full text available

Citations Cited by
19
A mild and efficient route to Schiff base derivatives of amino acids
A mild and efficient route to Schiff base derivatives of amino acids
Material Type:
Article 		Add to My Research

A mild and efficient route to Schiff base derivatives of amino acids

Journal of organic chemistry, 1982-06, Vol.47 (13), p.2663-2666 [Peer Reviewed Journal]

ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo00134a030

Full text available

Citations Cited by
20
Efficient Catalytic Enantioselective Reaction of a Glycine Cation Equivalent with Malonate Anions via Palladium Catalysis
Efficient Catalytic Enantioselective Reaction of a Glycine Cation Equivalent with Malonate Anions via Palladium Catalysis
Material Type:
Article 		Add to My Research

Efficient Catalytic Enantioselective Reaction of a Glycine Cation Equivalent with Malonate Anions via Palladium Catalysis

Journal of organic chemistry, 1997-06, Vol.62 (12), p.3962-3975 [Peer Reviewed Journal]

Copyright © 1997 American Chemical Society ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo961869w

Full text available

Citations Cited by

Results 1 - 20 of 63  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (45)

Refine My Results

Creation Date 

From To
Refine
  1. Before 1989  (13)
  2. 1989 To 1996  (16)
  3. 1997 To 2004  (18)
  4. 2005 To 2017  (9)
  5. After 2017  (8)
  6. More options open sub menu

Resource Type 

  1. Articles  (47)
  2. Patents  (16)
  3. More options open sub menu

Language 

  1. Japanese  (10)
  2. French  (4)
  3. More options open sub menu
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY (84-028) 37 755 057 Feedback
19 Nguyen Huu Tho St. Dist.7, HCM thuvien@tdtu.edu.vn

Copyright © 2017 INSPIRE LIBRARY - TON DUC THANG UNIVERSITY

Searching Remote Databases, Please Wait