Mechanistic studies on stereoselective domino [4 + 2]/retro[3 + 2]/[3 + 2] cycloaddition reactions of oxadiazoles with strained and unstrained cycloalkenes-Reference-Cited by-同舟云学术

Mechanistic studies on stereoselective domino [4 + 2]/retro[3 + 2]/[3 + 2] cycloaddition reactions of oxadiazoles with strained and unstrained cycloalkenes

Published:2022-02 Issue:2 Volume:141 Page:
ISSN:1432-881X
Container-title:Theoretical Chemistry Accounts
language:en
Short-container-title:Theor Chem Acc

Author:

Umar Abdul Rashid^ORCID,Opoku Ernest^ORCID

Funder

Nesvard Africa Science Project

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s00214-022-02872-y.pdf

Reference57 articles.

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3. Rodríguez JR, Rumbo A, Castedo L, Mascareñas JL (1999) Straightforward construction of fused 6,7,5-tricarbocyclic systems by tandem [5 + 2]/[4 + 2] cycloadditions. J Org Chem 64:966–970. https://doi.org/10.1021/jo982050g

4. Denmark SE, Seierstad M, Herbert B (1999) Tandem cycloaddition chemistry of nitroalkenes: preparative and theoretical studies on the stereochemical course of [3 + 2] cycloaddition of cyclic nitronates. J Org Chem 64:884–901. https://doi.org/10.1021/jo9818374

5. Denmark SE, Baiazitov RY, SED, Baiazitov RY, (2006) Tandem double-intramolecular [4 + 2]/[3 + 2] cycloadditions of nitroalkenes. Studies toward a total synthesis of daphnilactone B: piperidine ring construction. J Org Chem 71:593–605. https://doi.org/10.1021/jo052001l

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