Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine
Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether openin...
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1995 |
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| Umfang: |
4 |
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| Reproduktion: |
Springer Online Journal Archives 1860-2002 |
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| Übergeordnetes Werk: |
in: Russian chemical bulletin - 1952, 44(1995) vom: Mai, Seite 923-926 |
| Übergeordnetes Werk: |
volume:44 ; year:1995 ; month:05 ; pages:923-926 ; extent:4 |
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| 520 | |a Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. | ||
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(DE-627)NLEJ192223232 DE-627 ger DE-627 rakwb eng Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine 1995 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. Springer Online Journal Archives 1860-2002 Gromov, S. P. oth Vedernikov, A. I. oth Fedorova, O. A. oth in Russian chemical bulletin 1952 44(1995) vom: Mai, Seite 923-926 (DE-627)NLEJ188989994 (DE-600)2037677-7 1573-9171 nnns volume:44 year:1995 month:05 pages:923-926 extent:4 http://dx.doi.org/10.1007/BF00696929 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 44 1995 5 923-926 4 |
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(DE-627)NLEJ192223232 DE-627 ger DE-627 rakwb eng Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine 1995 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. Springer Online Journal Archives 1860-2002 Gromov, S. P. oth Vedernikov, A. I. oth Fedorova, O. A. oth in Russian chemical bulletin 1952 44(1995) vom: Mai, Seite 923-926 (DE-627)NLEJ188989994 (DE-600)2037677-7 1573-9171 nnns volume:44 year:1995 month:05 pages:923-926 extent:4 http://dx.doi.org/10.1007/BF00696929 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 44 1995 5 923-926 4 |
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(DE-627)NLEJ192223232 DE-627 ger DE-627 rakwb eng Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine 1995 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. Springer Online Journal Archives 1860-2002 Gromov, S. P. oth Vedernikov, A. I. oth Fedorova, O. A. oth in Russian chemical bulletin 1952 44(1995) vom: Mai, Seite 923-926 (DE-627)NLEJ188989994 (DE-600)2037677-7 1573-9171 nnns volume:44 year:1995 month:05 pages:923-926 extent:4 http://dx.doi.org/10.1007/BF00696929 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 44 1995 5 923-926 4 |
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(DE-627)NLEJ192223232 DE-627 ger DE-627 rakwb eng Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine 1995 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. Springer Online Journal Archives 1860-2002 Gromov, S. P. oth Vedernikov, A. I. oth Fedorova, O. A. oth in Russian chemical bulletin 1952 44(1995) vom: Mai, Seite 923-926 (DE-627)NLEJ188989994 (DE-600)2037677-7 1573-9171 nnns volume:44 year:1995 month:05 pages:923-926 extent:4 http://dx.doi.org/10.1007/BF00696929 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 44 1995 5 923-926 4 |
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(DE-627)NLEJ192223232 DE-627 ger DE-627 rakwb eng Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine 1995 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. Springer Online Journal Archives 1860-2002 Gromov, S. P. oth Vedernikov, A. I. oth Fedorova, O. A. oth in Russian chemical bulletin 1952 44(1995) vom: Mai, Seite 923-926 (DE-627)NLEJ188989994 (DE-600)2037677-7 1573-9171 nnns volume:44 year:1995 month:05 pages:923-926 extent:4 http://dx.doi.org/10.1007/BF00696929 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 44 1995 5 923-926 4 |
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macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine |
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Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine |
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Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. |
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Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. |
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Abstract A new method for synthesizing nitrogen-containing podands by nucleophilic regioselective cleavage of the macrocycle in formyl derivatives of benzocrown ethers by heating with methylamine and methylammonium chloride has been developed. This reaction is the first example of crown ether opening by a nitrogen-containing nucleophile. |
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Macrocycle opening in formyl derivatives of benzocrown ethers under the action of methylamine |
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