Although, the discovery process for a pharmaceutical product requires manag
ement of various biological sciences and organic synthesis, but once a comp
ound has satisfied therapeutic requirements and safety standards, the scien
ce involved is essentially organic synthesis, i.e. large-scale manufacture
of the compound. Since, any synthesis/manufacture in today's context ought
to be green, should not pollute the environment, has to be cost-effective,
adheres to safety standards and gives preference for specific stereoisomers
, the synthetic scheme one intends to adopt must satisfy and conform to the
se requirements. A. paradigm shift is taking place on how one develops a st
rategy for synthesis of complex molecules like drugs and fine chemicals. Ho
wever, many of the syntheses fall short of the requirements. This article r
eviews the advancement that is taking place in the area of organic synthesi
s, wherein the modern requirements such as syntheses : (a) achieved in one
step, (b) utilising non-hazardous and non-toxic chemicals, (c) which are re
source efficient, (d) which are essentially free of solvents and (e) which
are enatioselective are described with specific examples from the drugs and
fine chemicals sector.