Literature DB >> 22111917

Expanding the azaspiro[3.3]heptane family: synthesis of novel highly functionalized building blocks.

Johannes A Burkhard1, Carine Guérot, Henner Knust, Erick M Carreira.   

Abstract

The preparation of versatile azaspiro[3.3]heptanes carrying multiple exit vectors is disclosed. Expedient synthetic routes enable the straightforward access to these novel modules that are expected to have significance in drug discovery and design.
© 2011 American Chemical Society

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Year:  2011        PMID: 22111917     DOI: 10.1021/ol2028459

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  11 in total

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2.  Multigram Synthesis of Advanced 6,6-Difluorospiro[3.3]heptane-derived Building Blocks.

Authors:  Oleksandr S Olifir; Anton V Chernykh; Alexey V Dobrydnev; Oleksandr O Grygorenko; Yuriy S Moroz; Zoia V Voitenko; Dmytro S Radchenko
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3.  Catalytic Arylboration of Spirocyclic Cyclobutenes: Rapid Access to Highly Substituted Spiro[3.n]alkanes.

Authors:  Amit Kumar Simlandy; Mao-Yun Lyu; M Kevin Brown
Journal:  ACS Catal       Date:  2021-10-06       Impact factor: 13.700

4.  Synthesis of a family of spirocyclic scaffolds: building blocks for the exploration of chemical space.

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Journal:  J Org Chem       Date:  2013-06-26       Impact factor: 4.354

5.  Synthesis and profiling of a diverse collection of azetidine-based scaffolds for the development of CNS-focused lead-like libraries.

Authors:  Jason T Lowe; Maurice D Lee; Lakshmi B Akella; Emeline Davoine; Etienne J Donckele; Landon Durak; Jeremy R Duvall; Baudouin Gerard; Edward B Holson; Adrien Joliton; Sarathy Kesavan; Berenice C Lemercier; Haibo Liu; Jean-Charles Marié; Carol A Mulrooney; Giovanni Muncipinto; Morgan Welzel-O'Shea; Laura M Panko; Ann Rowley; Byung-Chul Suh; Meryl Thomas; Florence F Wagner; Jingqiang Wei; Michael A Foley; Lisa A Marcaurelle
Journal:  J Org Chem       Date:  2012-08-10       Impact factor: 4.354

6.  Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols.

Authors:  Thomas O Painter; Jonathon R Bunn; Frank J Schoenen; Justin T Douglas; Victor W Day; Conrad Santini
Journal:  J Org Chem       Date:  2013-04-01       Impact factor: 4.354

7.  Strain-Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones.

Authors:  Jasper L Tyler; Adam Noble; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2021-04-16       Impact factor: 15.336

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Authors:  F F Wagner; Y-L Zhang; D M Fass; N Joseph; J P Gale; M Weïwer; P McCarren; S L Fisher; T Kaya; W-N Zhao; S A Reis; K M Hennig; M Thomas; B C Lemercier; M C Lewis; J S Guan; M P Moyer; E Scolnick; S J Haggarty; L-H Tsai; E B Holson
Journal:  Chem Sci       Date:  2015-01-01       Impact factor: 9.825

9.  Carbamoyl radical-mediated synthesis and semipinacol rearrangement of β-lactam diols.

Authors:  Marie Betou; Louise Male; Jonathan W Steed; Richard S Grainger
Journal:  Chemistry       Date:  2014-04-07       Impact factor: 5.236

10.  Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp3)-O bond formation.

Authors:  Yechan Kim; Seoung-Tae Kim; Dahye Kang; Te-Ik Sohn; Eunyoung Jang; Mu-Hyun Baik; Sungwoo Hong
Journal:  Chem Sci       Date:  2017-11-27       Impact factor: 9.825

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