ALPHA-HYDROXYLAMINO NITRILES AND ALPHA-HYDROXYLAMINO ACIDS

[1] ABDERHALDEN E, 1921, CHEM ZENTR, V3, P296

[2] ADICKES F, 1943, J PRAKT CHEM, V161, P279

[3] ALPHA-OXIMINO ACID INTERMEDIATES FOR THE SYNTHESIS OF ALPHA-AMINO ACIDS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1947, 12 (03) : 460 - 468

[4] Divison of some racmic amino acids in optical active components [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1900, 33 : 2383 - 2393

[5] SYNTHESIS OF PEPTIDES VIA ALPHA-BENZYLOXIMINO ACIDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (08) : 2261 - 2262

[6] Technics in the synthesis of porphyrindin [J]. JOURNAL OF ORGANIC CHEMISTRY, 1942, 7 (02) : 164 - 168

[7] MARKO D, 1908, ANN, V362, P333

[8] NEELAKANTAN L, UNPUB

[9] alpha-hydroxylaminoisobutyronitrile - An intermediate in the synthesis of porphyrexide and porphyrindine [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1939, 61 : 754 - 754

[10] Porphyrexide and porphyrindine analogs derived from 1-hydroxyaminocyclohexyl cyanide [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1652 - 1655

[1] ABDERHALDEN E, 1921, CHEM ZENTR, V3, P296

[2] ADICKES F, 1943, J PRAKT CHEM, V161, P279

[3] ALPHA-OXIMINO ACID INTERMEDIATES FOR THE SYNTHESIS OF ALPHA-AMINO ACIDS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1947, 12 (03) : 460 - 468

[4] Divison of some racmic amino acids in optical active components [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1900, 33 : 2383 - 2393

[5] SYNTHESIS OF PEPTIDES VIA ALPHA-BENZYLOXIMINO ACIDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (08) : 2261 - 2262

[6] Technics in the synthesis of porphyrindin [J]. JOURNAL OF ORGANIC CHEMISTRY, 1942, 7 (02) : 164 - 168

[7] MARKO D, 1908, ANN, V362, P333

[8] NEELAKANTAN L, UNPUB

[9] alpha-hydroxylaminoisobutyronitrile - An intermediate in the synthesis of porphyrexide and porphyrindine [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1939, 61 : 754 - 754

[10] Porphyrexide and porphyrindine analogs derived from 1-hydroxyaminocyclohexyl cyanide [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1652 - 1655