Literature DB >> 12636378

New strategy for convergent steroid synthesis.

Olivier Lepage1, Pierre Deslongchamps.   

Abstract

We published recently our results on a new and convergent synthesis of natural steroids. The strategy was based on a cycloaddition reaction of Nazarov reagents 2 and 5 with cyclohexenones 1 and 4. In this paper we report results that deal with the synthesis of two new bicyclic Nazarov reagents (13 and 19) and their cycloaddition with two cyclohexenones (1 and 4). These new results constitute an important improvement concerning the versatility of the strategy since tetracycles having the stereochemistry found in natural steroids are now available.

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Year:  2003        PMID: 12636378     DOI: 10.1021/jo026676p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  From an ent-Estrane, through a nat-Androstane, to the Total Synthesis of the Marine-Derived Δ8,9-Pregnene (+)-03219A.

Authors:  Zachary A Shalit; Lucas C Valdes; Wan Shin Kim; Glenn C Micalizio
Journal:  Org Lett       Date:  2021-02-26       Impact factor: 6.005

Review 2.  A review on various aspects of organic synthesis using Comins' reagent.

Authors:  Duraipandi Devi Priya; Chetan Lakshman; Selvaraj Mohana Roopan
Journal:  Mol Divers       Date:  2021-01-03       Impact factor: 2.943

  2 in total

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