Diastereoselective Michael Additions of N-Boc-2-(tert-butyldimethylsiloxy)pyrrole to 2-(Arylsulfinyl)-1,4-benzoquinones-Reference-Cited by-同舟云学术

Diastereoselective Michael Additions of N-Boc-2-(tert-butyldimethylsiloxy)pyrrole to 2-(Arylsulfinyl)-1,4-benzoquinones

Published:2002-06-22 Issue:16 Volume:67 Page:5638-5643
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Arroyo Yolanda¹,de Paz Mónica¹,Rodríguez Justo F.¹,Sanz-Tejedor M. Ascensión¹,García Ruano José L.¹

Affiliation:

1. Departamento de Química Orgánica (E.T.S.I.I.), Universidad de Valladolid, Paseo del Cauce s/n, 47011-Valladolid, Spain, and Departamento de Química Orgánica (C-1), Universidad Autónoma de Madrid, Cantoblanco, 28049-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo016239v

Reference24 articles.

1. Influence of the Sulfinyl Group on the Chemoselectivity and π-Facial Selectivity of Diels−Alder Reactions of (S)-2-(p-Tolylsulfinyl)-1,4-benzoquinone

2. Enantioselective Diels–Alder Approach to Angucyclinones from(S)-2-(p-Tolylsulfinyl)-1,4-naphthoquinone and Substituted Racemic Vinylcyclohexenes

3. Short and efficient enantioselective total synthesis of angucyclinone type antibiotics (+)-rubiginone B2 and (+)-ochromycinone

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