SYNTHESES AND REACTIONS OF ACYCLIC N,N-DIACYLGLYCINES

[1] CLARKE HT, 1949, CHEMISTRY PENICIL ED, P781

[2] Colby C. E., 1891, AM CHEM J, V13, P1

[3] HARINGTON CR, 1936, BIOCH J, V30, P1609

[4] MUMM O, 1915, BER DTSCH CHEM GES, V48, P388

[5] The catalytic dehydrogenation of 2-substituted-5,6,7,8-tetrahydronaphthalene derivatives [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1943, 65 : 1097 - 1101

[6] RUGGLI P, 1929, HELV CHEM ACT, V12, P361

[7] THE TOTAL SYNTHESIS OF A 5-PHENYL PENICILLIN - METHYL 5-PHENYL-(2-CARBOMETHOXY-ETHYL)-PENICILLINATE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1950, 72 (08) : 3828 - 3829

[8] THE CONDENSATION PRODUCTS OF OXALYL CHLORIDE WITH MONOSUBSTITUTED AMIDES - STRUCTURE AND REACTIONS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (02) : 360 - 365

[9] A NEW SYNTHETIC ROUTE TO PEPTIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (05) : 1856 - 1861

[10] The hydrolysis of mixed secondary amides by alkalis. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1914, 105 : 299 - 309

[1] CLARKE HT, 1949, CHEMISTRY PENICIL ED, P781

[2] Colby C. E., 1891, AM CHEM J, V13, P1

[3] HARINGTON CR, 1936, BIOCH J, V30, P1609

[4] MUMM O, 1915, BER DTSCH CHEM GES, V48, P388

[5] The catalytic dehydrogenation of 2-substituted-5,6,7,8-tetrahydronaphthalene derivatives [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1943, 65 : 1097 - 1101

[6] RUGGLI P, 1929, HELV CHEM ACT, V12, P361

[7] THE TOTAL SYNTHESIS OF A 5-PHENYL PENICILLIN - METHYL 5-PHENYL-(2-CARBOMETHOXY-ETHYL)-PENICILLINATE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1950, 72 (08) : 3828 - 3829

[8] THE CONDENSATION PRODUCTS OF OXALYL CHLORIDE WITH MONOSUBSTITUTED AMIDES - STRUCTURE AND REACTIONS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (02) : 360 - 365

[9] A NEW SYNTHETIC ROUTE TO PEPTIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (05) : 1856 - 1861

[10] The hydrolysis of mixed secondary amides by alkalis. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1914, 105 : 299 - 309