Conformational control of bond migration in the D-homo rearrangement of 17-hydroxy-20-keto steroids

The concept of conformational control of bond migration in the trnsition state to theD-homo-annulation of 17-hydroxy-20-keto steroids appears to provide a unified rationale for the observed phenomena.Contribution from Merck & Co., Inc., Rahway, N. J., presented before the North Jersey Section of the American Chemical Society byN. L. Wendler as part of a lecture entitledStereochemical Effects AttendingD-Ring Rearrangements in Steroids, February 3, 1959.