Amino-Protecting Groups Subject to Deblocking under Conditions of Nucleophilic Addition to a Michael Acceptor. Structure−Reactivity Studies and Use of the 2-(tert-Butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) Group-Reference-Cited by-同舟云学术

Amino-Protecting Groups Subject to Deblocking under Conditions of Nucleophilic Addition to a Michael Acceptor. Structure−Reactivity Studies and Use of the 2-(tert-Butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) Group

Published:1999-05-19 Issue:12 Volume:64 Page:4315-4323
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Carpino Louis A.¹,Philbin Michael¹

Affiliation:

1. Department of Chemistry, Box 34510, University of Massachusetts, Amherst, Massachusetts 01003-4510

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982141d

Reference41 articles.

1. New Family of Base- and Nucleophile-Sensitive Amino-Protecting Groups. A Michael-Acceptor-Based Deblocking Process. Practical Utilization of the 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Group

2. Silicon in organic synthesis. 24. Preparation and selected reactions of functionalized 1-(trimethylsilyl)-substituted cyclopropanes

3. Aldol Reactions of Formaldehyde in Non-aqueous Media. II. Base-catalyzed Reaction of Fluorene and Nitrotoluenes with Formaldehyde in Dimethyl Sulfoxide.

4. Cytotoxic compounds. Part XIX. Allylic rearrangements in the reactions of 3-(phenylthio)prop-2-enyl chloride, 3-(p-nitrophenylthio)prop-2-enyl methanesulphonate, and 3-(p-nitrophenylthio)prop-2-enyl chloride with nucleophiles

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