A novel method for the preparation of peptidyl α-keto esters
A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain.
Gespeichert in:
| Autor*in: |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1990 |
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| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
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| Übergeordnetes Werk: |
in: Tetrahedron Letters - Amsterdam : Elsevier, 31(1990), 10, Seite 1385-1388 |
| Übergeordnetes Werk: |
volume:31 ; year:1990 ; number:10 ; pages:1385-1388 |
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| 520 | |a A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. | ||
| 520 | |a Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. | ||
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(DE-627)NLEJ176307753 (DE-599)GBVNLZ176307753 DE-627 ger DE-627 rakwb eng A novel method for the preparation of peptidyl α-keto esters 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Burkhart, J.P. oth Peet, N.P. oth Bey, P. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 10, Seite 1385-1388 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:10 pages:1385-1388 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88812-7 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 10 1385-1388 |
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(DE-627)NLEJ176307753 (DE-599)GBVNLZ176307753 DE-627 ger DE-627 rakwb eng A novel method for the preparation of peptidyl α-keto esters 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Burkhart, J.P. oth Peet, N.P. oth Bey, P. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 10, Seite 1385-1388 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:10 pages:1385-1388 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88812-7 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 10 1385-1388 |
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(DE-627)NLEJ176307753 (DE-599)GBVNLZ176307753 DE-627 ger DE-627 rakwb eng A novel method for the preparation of peptidyl α-keto esters 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Burkhart, J.P. oth Peet, N.P. oth Bey, P. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 10, Seite 1385-1388 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:10 pages:1385-1388 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88812-7 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 10 1385-1388 |
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(DE-627)NLEJ176307753 (DE-599)GBVNLZ176307753 DE-627 ger DE-627 rakwb eng A novel method for the preparation of peptidyl α-keto esters 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Burkhart, J.P. oth Peet, N.P. oth Bey, P. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 10, Seite 1385-1388 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:10 pages:1385-1388 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88812-7 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 10 1385-1388 |
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(DE-627)NLEJ176307753 (DE-599)GBVNLZ176307753 DE-627 ger DE-627 rakwb eng A novel method for the preparation of peptidyl α-keto esters 1990 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Burkhart, J.P. oth Peet, N.P. oth Bey, P. oth in Tetrahedron Letters Amsterdam : Elsevier 31(1990), 10, Seite 1385-1388 (DE-627)NLEJ175981779 (DE-600)2007074-3 0040-4039 nnns volume:31 year:1990 number:10 pages:1385-1388 http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88812-7 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 31 1990 10 1385-1388 |
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A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. |
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A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. |
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A new method for the synthesis of peptidyl α-keto esters is described, which is particularly useful for the construction of proteinase inhibitors with a lysine side chain. Addition of an acyloxy anion equivalent to a differentially protected lysinal was the key step in the preparation of 8. This new synthesis of α-keto esters is useful for the preparation of proteinase inhibitors with a lysine sidechain. |
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