Neurosteroid analogues. Part 13: Synthetic methods for the preparation of 2β-hydroxygonane derivatives as structural mimics of ent-3α-hydroxysteroid modulators of GABAA receptors

Cunde Wang; Nigam P. Rath; Douglas F. Covey

doi:10.1016/j.tet.2007.05.068

Neurosteroid analogues. Part 13: Synthetic methods for the preparation of 2β-hydroxygonane derivatives as structural mimics of ent-3α-hydroxysteroid modulators of GABAA receptors

Cunde Wang, Nigam P. Rath, Douglas F. Covey

University of Missouri-St. Louis

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Tetrahedron
Volume	63
DOIs	https://doi.org/10.1016/j.tet.2007.05.068
State	Published - Aug 1 2007

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Chemistry

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title = "Neurosteroid analogues. Part 13: Synthetic methods for the preparation of 2β-hydroxygonane derivatives as structural mimics of ent-3α-hydroxysteroid modulators of GABAA receptors",

author = "Cunde Wang and Rath, {Nigam P.} and Covey, {Douglas F.}",

note = "Many different 3α-hydroxysteroids in the androstane and pregnane steroid series enhance the actions of γ-aminobutyric acid (GABA) at GABA type-A (GABA...",

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AU - Wang, Cunde

AU - Rath, Nigam P.

AU - Covey, Douglas F.

N1 - Many different 3α-hydroxysteroids in the androstane and pregnane steroid series enhance the actions of γ-aminobutyric acid (GABA) at GABA type-A (GABA...

PY - 2007/8/1

Y1 - 2007/8/1

UR - https://www.sciencedirect.com/science/article/pii/S0040402007009362

U2 - 10.1016/j.tet.2007.05.068

DO - 10.1016/j.tet.2007.05.068

M3 - Article

VL - 63

JO - Tetrahedron

JF - Tetrahedron

ER -

Neurosteroid analogues. Part 13: Synthetic methods for the preparation of 2β-hydroxygonane derivatives as structural mimics of ent-3α-hydroxysteroid modulators of GABAA receptors

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