Strecker amino acid synthesis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Strecker amino acid synthesis" in English language version.

refsWebsite

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17doi.org

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9nih.gov

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3harvard.edu

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17^th place

2zenodo.org

621^st place

380^th place

1semanticscholar.org

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1worldcat.org

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doi.org

"dl-Alanine". Organic Syntheses. 9: 4. 1929. doi:10.15227/orgsyn.009.0004.
"a-Aminoisobutyric Acid". Organic Syntheses. 11: 4. 1931. doi:10.15227/orgsyn.011.0004.
Drauz, Karlheinz; Grayson, Ian; Kleemann, Axel; Krimmer, Hans-Peter; Leuchtenberger, Wolfgang; Weckbecker, Christoph (2006). "Amino Acids". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_057.pub2. ISBN 978-3-527-30673-2.
Masumoto, Shuji; Usuda, Hiroyuki; Suzuki, Masato; Kanai, Motomu; Shibasaki, Masakatsu (May 2003). "Catalytic Enantioselective Strecker Reaction of Ketoimines". Journal of the American Chemical Society. 125 (19): 5634–5635. doi:10.1021/ja034980+. PMID 12733893.
Kuethe, Jeffrey T.; Gauthier, Donald R.; Beutner, Gregory L.; Yasuda, Nobuyoshi (September 2007). "A Concise Synthesis of (S)-N-Ethoxycarbonyl-α-methylvaline". The Journal of Organic Chemistry. 72 (19): 7469–7472. doi:10.1021/jo7012862. PMID 17713956.
Wang, Jun; Liu, Xiaohua; Feng, Xiaoming (9 November 2011). "Asymmetric Strecker Reactions". Chemical Reviews. 111 (11): 6947–6983. doi:10.1021/cr200057t. PMID 21851054.
Zuend, Stephan J.; Coughlin, Matthew P.; Lalonde, Mathieu P.; Jacobsen, Eric N. (October 2009). "Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids". Nature. 461 (7266): 968–970. Bibcode:2009Natur.461..968Z. doi:10.1038/nature08484. PMC 2778849. PMID 19829379.
Yan, Hailong; Suk Oh, Joong; Lee, Ji-Woong; Eui Song, Choong (20 November 2012). "Scalable organocatalytic asymmetric Strecker reactions catalysed by a chiral cyanide generator". Nature Communications. 3 (1): 1212. Bibcode:2012NatCo...3.1212Y. doi:10.1038/ncomms2216. PMID 23169053.
Strecker, Adolph (1850). "Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper". Annalen der Chemie und Pharmacie. 75 (1): 27–45. doi:10.1002/jlac.18500750103.
Strecker, Adolph (1854). "Ueber einen neuen aus Aldehyd - Ammoniak und Blausäure entstehenden Körper". Annalen der Chemie und Pharmacie. 91 (3): 349–351. doi:10.1002/jlac.18540910309.
Davis, Franklin A.; Reddy, Rajarathnam E.; Portonovo, Padma S. (December 1994). "Asymmetric strecker synthesis using enantiopure sulfinimines: A convenient synthesis of α-amino acids". Tetrahedron Letters. 35 (50): 9351–9354. doi:10.1016/S0040-4039(00)78540-6.
Ishitani, Haruro; Komiyama, Susumu; Hasegawa, Yoshiki; Kobayashi, Shū (February 2000). "Catalytic Asymmetric Strecker Synthesis. Preparation of Enantiomerically Pure α-Amino Acid Derivatives from Aldimines and Tributyltin Cyanide or Achiral Aldehydes, Amines, and Hydrogen Cyanide Using a Chiral Zirconium Catalyst". Journal of the American Chemical Society. 122 (5): 762–766. doi:10.1021/ja9935207.
Huang, Jinkun; Corey, E. J. (December 2004). "A New Chiral Catalyst for the Enantioselective Strecker Synthesis of α-Amino Acids". Organic Letters. 6 (26): 5027–5029. doi:10.1021/ol047698w. PMID 15606127.
Harada, Kaoru (December 1963). "Asymmetric Synthesis of α-Amino-acids by the Strecker Synthesis". Nature. 200 (4912): 1201. Bibcode:1963Natur.200.1201H. doi:10.1038/2001201a0. PMID 14089910. S2CID 43857409.
Iyer, Mani S.; Gigstad, Kenneth M.; Namdev, Nivedita D.; Lipton, Mark (January 1996). "Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide". Journal of the American Chemical Society. 118 (20): 4910–4911. doi:10.1021/ja952686e. PMID 24178715.
Iyer, Mani S.; Gigstad, Kenneth M.; Namdev, Nivedita D.; Lipton, Mark (2023-06-29). "Retraction of "Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide″". Journal of the American Chemical Society. doi:10.1021/jacs.3c03705. ISSN 0002-7863.
Duthaler, Rudolf O. (January 1994). "Recent developments in the stereoselective synthesis of α-aminoacids". Tetrahedron. 50 (6): 1539–1650. doi:10.1016/S0040-4020(01)80840-1.

harvard.edu

ui.adsabs.harvard.edu

Zuend, Stephan J.; Coughlin, Matthew P.; Lalonde, Mathieu P.; Jacobsen, Eric N. (October 2009). "Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids". Nature. 461 (7266): 968–970. Bibcode:2009Natur.461..968Z. doi:10.1038/nature08484. PMC 2778849. PMID 19829379.
Yan, Hailong; Suk Oh, Joong; Lee, Ji-Woong; Eui Song, Choong (20 November 2012). "Scalable organocatalytic asymmetric Strecker reactions catalysed by a chiral cyanide generator". Nature Communications. 3 (1): 1212. Bibcode:2012NatCo...3.1212Y. doi:10.1038/ncomms2216. PMID 23169053.
Harada, Kaoru (December 1963). "Asymmetric Synthesis of α-Amino-acids by the Strecker Synthesis". Nature. 200 (4912): 1201. Bibcode:1963Natur.200.1201H. doi:10.1038/2001201a0. PMID 14089910. S2CID 43857409.

nih.gov

pubmed.ncbi.nlm.nih.gov

Masumoto, Shuji; Usuda, Hiroyuki; Suzuki, Masato; Kanai, Motomu; Shibasaki, Masakatsu (May 2003). "Catalytic Enantioselective Strecker Reaction of Ketoimines". Journal of the American Chemical Society. 125 (19): 5634–5635. doi:10.1021/ja034980+. PMID 12733893.
Kuethe, Jeffrey T.; Gauthier, Donald R.; Beutner, Gregory L.; Yasuda, Nobuyoshi (September 2007). "A Concise Synthesis of (S)-N-Ethoxycarbonyl-α-methylvaline". The Journal of Organic Chemistry. 72 (19): 7469–7472. doi:10.1021/jo7012862. PMID 17713956.
Wang, Jun; Liu, Xiaohua; Feng, Xiaoming (9 November 2011). "Asymmetric Strecker Reactions". Chemical Reviews. 111 (11): 6947–6983. doi:10.1021/cr200057t. PMID 21851054.
Zuend, Stephan J.; Coughlin, Matthew P.; Lalonde, Mathieu P.; Jacobsen, Eric N. (October 2009). "Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids". Nature. 461 (7266): 968–970. Bibcode:2009Natur.461..968Z. doi:10.1038/nature08484. PMC 2778849. PMID 19829379.
Yan, Hailong; Suk Oh, Joong; Lee, Ji-Woong; Eui Song, Choong (20 November 2012). "Scalable organocatalytic asymmetric Strecker reactions catalysed by a chiral cyanide generator". Nature Communications. 3 (1): 1212. Bibcode:2012NatCo...3.1212Y. doi:10.1038/ncomms2216. PMID 23169053.
Huang, Jinkun; Corey, E. J. (December 2004). "A New Chiral Catalyst for the Enantioselective Strecker Synthesis of α-Amino Acids". Organic Letters. 6 (26): 5027–5029. doi:10.1021/ol047698w. PMID 15606127.
Harada, Kaoru (December 1963). "Asymmetric Synthesis of α-Amino-acids by the Strecker Synthesis". Nature. 200 (4912): 1201. Bibcode:1963Natur.200.1201H. doi:10.1038/2001201a0. PMID 14089910. S2CID 43857409.
Iyer, Mani S.; Gigstad, Kenneth M.; Namdev, Nivedita D.; Lipton, Mark (January 1996). "Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide". Journal of the American Chemical Society. 118 (20): 4910–4911. doi:10.1021/ja952686e. PMID 24178715.

ncbi.nlm.nih.gov

Zuend, Stephan J.; Coughlin, Matthew P.; Lalonde, Mathieu P.; Jacobsen, Eric N. (October 2009). "Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids". Nature. 461 (7266): 968–970. Bibcode:2009Natur.461..968Z. doi:10.1038/nature08484. PMC 2778849. PMID 19829379.

semanticscholar.org

api.semanticscholar.org

Harada, Kaoru (December 1963). "Asymmetric Synthesis of α-Amino-acids by the Strecker Synthesis". Nature. 200 (4912): 1201. Bibcode:1963Natur.200.1201H. doi:10.1038/2001201a0. PMID 14089910. S2CID 43857409.

worldcat.org

search.worldcat.org

Iyer, Mani S.; Gigstad, Kenneth M.; Namdev, Nivedita D.; Lipton, Mark (2023-06-29). "Retraction of "Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide″". Journal of the American Chemical Society. doi:10.1021/jacs.3c03705. ISSN 0002-7863.

zenodo.org

Strecker, Adolph (1850). "Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper". Annalen der Chemie und Pharmacie. 75 (1): 27–45. doi:10.1002/jlac.18500750103.
Strecker, Adolph (1854). "Ueber einen neuen aus Aldehyd - Ammoniak und Blausäure entstehenden Körper". Annalen der Chemie und Pharmacie. 91 (3): 349–351. doi:10.1002/jlac.18540910309.