Diastereo- and regioselective petasis aryl and allyl boration of ninhydrins towards synthesis of functionalized indene-diones and dihydrobenzoindeno-oxazin-ones-Reference-Cited by-同舟云学术

Diastereo- and regioselective petasis aryl and allyl boration of ninhydrins towards synthesis of functionalized indene-diones and dihydrobenzoindeno-oxazin-ones

Published:2022-08-01 Issue: Volume: Page:
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Sengupta Ayon,Maity Suvendu,Saha Pinaki,Ghosh Prasanta,Rudra Sonali,Mukhopadhyay Chhanda^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-022-10496-4.pdf

Reference83 articles.

1. Petasis NA, Akritopoulou I (1993) The boronic acid mannich reaction: a new method for the synthesis of geometrically pure allylamines. Tetrahedron Lett 34:583–586. https://doi.org/10.1016/S0040-4039(00)61625-8

2. Petasis NA, Zavialov I (1997) A new and practical synthesis of α-amino acids from alkenyl boronic acids. J Am Chem Soc 119:445–446. https://doi.org/10.1021/ja963178n

3. Petasis NA, Boral S (2001) One-step three-component reaction among organoboronic acids, amines and salicylaldehydes. Tetrahedron Lett 42:539–542. https://doi.org/10.1016/S0040-4039(00)02014-1

4. Muncipinto G, Moquist PN, Schreiber SL, Schaus SE (2011) Catalytic diastereoselective petasis reactions. Angew Chem Int Ed 50:8172–8175. https://doi.org/10.1002/anie.201103271

5. Li Y, Xu M-H (2012) Lewis acid promoted highly diastereoselective PetasisBorono-Mannich reaction: efficient synthesis of optically active β, γ-unsaturated α-amino acids. Org Lett 14:2062–2065. https://doi.org/10.1021/ol300581n