Amino Acid Mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a Seven-Membered Ring: Remarkable Inversion of Enantioselectivity Compared to the Six-Membered Ring Example-Reference-Cited by-同舟云学术

Amino Acid Mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a Seven-Membered Ring: Remarkable Inversion of Enantioselectivity Compared to the Six-Membered Ring Example

Published:2006-12-05 Issue:1 Volume:72 Page:123-131
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nagamine Takashi¹,Inomata Kohei¹,Endo Yasuyuki¹,Paquette Leo A.¹

Affiliation:

1. Tohoku Pharmaceutical University, 4-4-1 Komatsushima Aoba-ku, Sendai 981-8558 Japan, and Evans Chemical Laboratories, The Ohio State University, Columbus, Ohio 43210

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061824n

Reference65 articles.

1. Neuartige asymmetrische Cyclisierung zu optisch aktiven Steroid-CD-Teilstücken

2. Stereocontrolled synthesis of trans-hydrindan steroidal intermediates

3. Asymmetric synthesis of bicyclic intermediates of natural product chemistry

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