A STABLE CHLOROFORM ADDUCT OF 11-EPI-17-ALPHA-HYDROXYCORTICOSTERONE

[1] STEROIDAL CYCLIC KETALS .3. HYDROCORTISONE AND RELATED CORTICOIDS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1953, 18 (01) : 70 - 82

[2] STEROIDAL CYCLIC KETALS .4. THE CONVERSION OF 11-KETO-HYDROXYSTEROIDS TO 11-ALPHA-HYDROXYSTEROIDS - THE PREPARATION OF 11-EPI-HYDROCORTISONE, AND DELTA-4-ANDROSTENE-11-ALPHA-OL-3,17-DIONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1481 - 1482

[3] OXIDATION OF STEROIDS BY MICROORGANISMS .2. HYDROXYLATION IN POSITION 11 AND SYNTHESIS OF CORTISONE FROM REICHSTEINS COMPOUND-S [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (15) : 3962 - 3963

[4] 11-ALPHA-HYDROXYSTEROIDS - SYNTHESIS OF DELTA4-PREGNEN-11-ALPHA,17-ALPHA,21-TRIOL-3,20-DIONE 11,21-DIACETATE (11-EPI-COMPOUND-F DIACETATE) [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (17) : 4470 - 4471

[5] LARDON A, 1952, Pharm Acta Helv, V27, P287

[6] MICROBIOLOGICAL TRANSFORMATIONS OF STEROIDS .4. THE 11-EPIMER OF COMPOUND-F AND OTHER NEW OXYGENATED DERIVATIVES OF REICHSTEIN COMPOUND-S - A NEW ROUTE TO CORTISONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (02) : 412 - 415

[7] ROMO J, 1952, CHEM IND-LONDON, P783

[8] STEROIDS .41. SYNTHESIS OF 11-ALPHA,17-ALPHA-DIHYDROXYPROGESTERONE AND OF 11-ALPHA,17-ALPHA,21-TRIHYDROXYPROGESTERONE, THE 11-EPIMER OF KENDALL COMPOUND-F [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1277 - 1282

[9] ROMO J, 1952, CHEM IND, P834

[10] INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .7. STEROIDS .42. STEROIDAL SAPOGENINS .26. THE CHEMICAL REDUCTION OF DELTA-8-11-KETO AND OF SATURATED 11-KETO STEROIDS - A NEW APPROACH TO 11-KETO AND 11-ALPHA-HYDROXY STEROIDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1282 - 1285

[1] STEROIDAL CYCLIC KETALS .3. HYDROCORTISONE AND RELATED CORTICOIDS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1953, 18 (01) : 70 - 82

[2] STEROIDAL CYCLIC KETALS .4. THE CONVERSION OF 11-KETO-HYDROXYSTEROIDS TO 11-ALPHA-HYDROXYSTEROIDS - THE PREPARATION OF 11-EPI-HYDROCORTISONE, AND DELTA-4-ANDROSTENE-11-ALPHA-OL-3,17-DIONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1481 - 1482

[3] OXIDATION OF STEROIDS BY MICROORGANISMS .2. HYDROXYLATION IN POSITION 11 AND SYNTHESIS OF CORTISONE FROM REICHSTEINS COMPOUND-S [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (15) : 3962 - 3963

[4] 11-ALPHA-HYDROXYSTEROIDS - SYNTHESIS OF DELTA4-PREGNEN-11-ALPHA,17-ALPHA,21-TRIOL-3,20-DIONE 11,21-DIACETATE (11-EPI-COMPOUND-F DIACETATE) [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (17) : 4470 - 4471

[5] LARDON A, 1952, Pharm Acta Helv, V27, P287

[6] MICROBIOLOGICAL TRANSFORMATIONS OF STEROIDS .4. THE 11-EPIMER OF COMPOUND-F AND OTHER NEW OXYGENATED DERIVATIVES OF REICHSTEIN COMPOUND-S - A NEW ROUTE TO CORTISONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (02) : 412 - 415

[7] ROMO J, 1952, CHEM IND-LONDON, P783

[8] STEROIDS .41. SYNTHESIS OF 11-ALPHA,17-ALPHA-DIHYDROXYPROGESTERONE AND OF 11-ALPHA,17-ALPHA,21-TRIHYDROXYPROGESTERONE, THE 11-EPIMER OF KENDALL COMPOUND-F [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1277 - 1282

[9] ROMO J, 1952, CHEM IND, P834

[10] INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .7. STEROIDS .42. STEROIDAL SAPOGENINS .26. THE CHEMICAL REDUCTION OF DELTA-8-11-KETO AND OF SATURATED 11-KETO STEROIDS - A NEW APPROACH TO 11-KETO AND 11-ALPHA-HYDROXY STEROIDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1282 - 1285