The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group: Towards the synthesis of 5α- and 5β-oriented Δ3-isomers of desogestrel-Reference-Cited by-同舟云学术

The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group: Towards the synthesis of 5α- and 5β-oriented Δ3-isomers of desogestrel

Published:1998-01 Issue:1 Volume:63 Page:21-27
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Ring Sven,Weber Gisela,Hillisch Alexander,Schwarz Sigfrid

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference19 articles.

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4. Gaussian 94 (Revision D.1), Frisch MJ, Trucks GW, Schlegel HB, Gill PMW, Johnson BG, Robb MA, Cheeseman JR, Keith TA, Petersson GA, Montgomery JA, Raghavachari K, Al-Laham MA, Zakrzewski VG, Ortiz JV, Foresman JB, Cioslowski J, Stefanov BB, Nanayakkara A, Challacombe M, Peng CY, Ayala PY, Chen W, Wong MW, Andres JL, Replogle ES, Gomperts R, Martin RL, Fox DJ, Binkley JS, Defrees DJ, Baker J, Steward JP, Head-Gordon M, Gonzales C, Pople JA, Gaussian, Inc. Pittsburgh PA, 1995.

5. SYBYL, Molecular Modeling System, Version 6.3, (1996), Tripos Associates, Inc., St. Louis, MO.

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3. Steroids: reactions and partial synthesis (1998);Natural Product Reports;2000