Chemical synthesis of 7- and 8-dehydro derivatives of pregnane-3,17α,20-triols, potential steroid metabolites in Smith–Lemli–Opitz syndrome
- 31 January 2003
- journal article
- Published by Elsevier BV in Steroids
- Vol. 68 (1), 31-42
- https://doi.org/10.1016/s0039-128x(02)00113-7
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Adrenal insufficiency and hypertension in a newborn infant with Smith-Lemli-Opitz syndromeAmerican Journal of Medical Genetics, 2001
- Synthesis of Ring B Unsaturated Estriols. Confirming the Structure of a Diagnostic Analyte for Smith−Lemli−Opitz SyndromeOrganic Letters, 2001
- Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndromePrenatal Diagnosis, 2001
- The Smith-Lemli-Opitz syndromeJournal of Medical Genetics, 2000
- Midgestational maternal urine steroid markers of fetal Smith–Lemli–Opitz (SLO) syndrome (7-dehydrocholesterol 7-reductase deficiency)Steroids, 1999
- Defective Cholesterol Biosynthesis Associated with the Smith-Lemli-Opitz SyndromeNew England Journal of Medicine, 1994
- Genetic Diseases of Steroid MetabolismPublished by Elsevier BV ,1994
- Genetic Disorders of Adrenal Hormone SynthesisHormone Research, 1992
- Reduction of 17.alpha.-hydroxy-20-keto steroids: convenient synthesis of (E)-3.beta.-hydroxy-5,17(20)-pregnadiene 3-pivaloate and (Z)-3.beta.,16.alpha.-dihydroxy-5,17(20)-pregnadiene 3-pivaloateThe Journal of Organic Chemistry, 1990
- The Saga of the Ring B Unsaturated Equine Estrogens*Endocrine Reviews, 1988