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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 20, 1990 - Issue 20
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Original Articles

Side-Chain Introduction In 16β-Acetoxy-17-oxo-androstanes

Darío Doller Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires. Ciudad Universitaria, Pab. II, (1428) Buenos Aires, Argentina; Department of Chemistry, Texas A&M University, College Station, TX, 77843-3255, U.S.A.
&
Eduardo G. Gros Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires. Ciudad Universitaria, Pab. II, (1428) Buenos Aires, Argentina
Pages 3115-3124 | Received 08 Aug 1990, Published online: 24 Oct 2006

Citations (9)

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Read on this site (2)

AndreaC. Bruttomesso, Darío Doller & EduardoG Gros. (1998) Stereospecific Synthesis of Steroidal 20,16-γ-Carbolactones. Synthetic Communications 28:21, pages 4043-4057.
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GustavoA. Revelli & EduardoG. Gros. (1993) A Facile Synthesis of 4-(3β -Methoxy-5α-androstan-17β-YL)-3-pyrrolin-2-one. Synthetic Communications 23:8, pages 1111-1119.
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Articles from other publishers (7)

Bingfeng Shi, Pingping Tang, Xiaoyi Hu, Jun O. Liu & Biao Yu. (2005) OSW Saponins:  Facile Synthesis toward a New Type of Structures with Potent Antitumor Activities. The Journal of Organic Chemistry 70:25, pages 10354-10367.
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Bingfeng Shi, Hao Wu, Biao Yu & Jiarui Wu. (2004) 23‐Oxa‐Analogues of OSW‐1: Efficient Synthesis and Extremely Potent Antitumor Activity. Angewandte Chemie International Edition 43:33, pages 4324-4327.
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Bingfeng Shi, Hao Wu, Biao Yu & Jiarui Wu. (2004) 23‐Oxa‐Analogues of OSW‐1: Efficient Synthesis and Extremely Potent Antitumor Activity. Angewandte Chemie 116:33, pages 4424-4427.
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Andrea C Bruttomesso, Darı́o Doller & Eduardo G Gros. (1999) Mechanistic studies of the rearrangements of steroidal 16,17-ketols and syntheses of 20→16-cis-γ-carbolactones. Bioorganic & Medicinal Chemistry 7:5, pages 943-947.
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Alicia Baldessari, Andrea C. Bruttomesso & Eduardo G. Gros. (2004) Lipase‐Catalysed Regioselective Deacetylation of androstane derivatives. Helvetica Chimica Acta 79:4, pages 999-1004.
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D. DOLLER & E. G. GROS. (2010) ChemInform Abstract: Side‐Chain Introduction in 16β‐Acetoxy‐17‐oxoandrostanes.. ChemInform 22:15.
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Darío Doller & Eduardo G. Gros. (1991) Carbon-13 nuclear magnetic resonance spectral data of steroidal vicinal ketols and related compounds. Steroids 56:4, pages 168-172.
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