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The Graduate School and University Center of The City University of New York

A Stereospecific Pd-Catalyzed Suzuki Cross-Coupling Reaction and a Statistical Study of the Ligand's Role in Stereoselection

Abstract

dc:description.abstract

<p>The development of palladium-catalyzed carbon-carbon cross-coupling reactions has profoundly influenced the manner through which we approach the synthesis of complex organic molecules. Among established cross-coupling reactions, which include Kumada, Negishi, and Stille reactions, the Suzuki cross-coupling reaction exhibits particularly wide functional group compatibility, while employing non-toxic, air-stable organoboron nucleophiles. Conventional studies of Pd-catalyzed Suzuki cross-coupling reactions have focused on C(sp<sup>2</sup>)-C(sp<sup>2</sup>) cross-coupling reactions, which result in the formation of planar products. Conceptually, the use of C(sp<sup>3</sup>) (secondary) nucleophiles would enable the reliable manipulation of organic molecules in three dimensions. However, this process has not been achievable due to the slow rate of transmetallation of secondary alkylboron nucleophiles, and the subsequent isomerization of alkyl units following transmetallation to palladium. Herein, we describe the development of a general process for Pd-catalyzed cross-coupling reactions involving alkylboron nucleophiles using racemic and enantioenriched alkylboron nucleophiles. The origin of stereoselectivity was investigated through correlation of parameterized phosphine properties to stereochemical outcomes. A stereodivergent cross-coupling reaction was developed in which stereoretention and stereoinversion could be selectively achieved through the proper choice of ligand. A broad range of aryl chloride or bromide and inactivated secondary alkylboron nucleophiles are applicable in these reactions.</p>

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy
Level thesis:degree_level
Doctoral
Discipline thesis:degree_discipline
Chemistry
Grantor
The Graduate School and University Center of The City University of New York
Year dc:date.available
2018

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Zhao, Shibin
Advisor dc:contributor.advisor
  • Mark R. Biscoe
Committee members dc:contributor.committeemember
  • Shengping Zheng
  • Akira Kawamura

Subjects

dc:subject × 5

Identifiers

dc:identifier.*
Repository record dc:identifier
https://academicworks.cuny.edu/gc_etds/2832
OAI identifier oai:identifier
oai:academicworks.cuny.edu:gc_etds-3897

Chain of custody

source
Harvested from
City University of New York - Graduate Center
Base URL
academicworks.cuny.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Zhao, Shibin. A Stereospecific Pd-Catalyzed Suzuki Cross-Coupling Reaction and a Statistical Study of the Ligand's Role in Stereoselection. Doctoral thesis, The Graduate School and University Center of The City University of New York, 2018. https://academicworks.cuny.edu/gc_etds/2832